Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3006104191

FEI Number

3006104191

Entity Name

AirStrip Technologies, Inc.

City/State/Country

SAN ANTONIO, TX, US

Establishment Address

2915 W Bitters Rd., Suite 215, SAN ANTONIO, TX 78248, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

AirStrip Technologies (Owner Number: 9065519)

Owner / Operator Contact Address

2915 W. Bitters Rd., Suite 215, San Antonio, TX 78248, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K090269

PMA Number

N/A

All Registered Proprietary Names

AirStrip AHI AirStrip ONE Web client AirStrip InsightIQ AirStrip AHI AirStrip AHI AIRSTRIP PATIENT MONITORING AirStrip OB

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
QNV	Adjunctive Hemodynamic Indicator With Decision Point	Cardiovascular	Class 2	870.2220	2025-05-19
QNL	Medium-Term Adjunctive Predictive Cardiovascular Indicator	Cardiovascular	Class 2	870.2210	2025-05-19
MSX	System, Network And Communication, Physiological Monitors	Cardiovascular	Class 2	870.2300	2017-01-06
MWI	Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)	Cardiovascular	Class 2	870.2300	2025-02-03
QNV	Adjunctive Hemodynamic Indicator With Decision Point	Cardiovascular	Class 2	870.2220	2025-05-19
QNL	Medium-Term Adjunctive Predictive Cardiovascular Indicator	Cardiovascular	Class 2	870.2210	2025-05-19
QNV	Adjunctive Hemodynamic Indicator With Decision Point	Cardiovascular	Class 2	870.2220	2025-05-19
MWI	Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)	Cardiovascular	Class 2	870.2300	2011-09-01
HGM	System, Monitoring, Perinatal	Obstetrics/Gynecology	Class 2	884.2740	2017-10-04

Official Correspondent

Shaconii Abraham

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

AirStrip Technologies

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K973527	Data Critical Corp.	CARDIO-PAGER SYSTEM	1998-03-31
K182637	Philips Medizin Systeme Boeblingen GmbH	Philips IntelliVue XDS Software	2019-04-26
K071802	Mammendorfer Institut Fur Physik Und Medizin GmbH	TESLA GUARD, MODEL EFT G04	2007-11-09
K124061	Invivo Corporation	MRI PATIENT MONITORING SYSTEM (MODEL 865214)	2013-02-22
K101264	Remote Diagnostic Technologies , Ltd.	TEMPUS IC PROFESSIONAL PATIENT MONITOR	2010-05-11

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0001-2015	Invivo Corporation	2	Philips Expression MR200 MRI Patient Monitoring System Model 866120
Z-0004-2023	Philips North America Llc	2	MR Patient Care Portal 5000 (Desktop Unit), Model Number 453564792561 This is a component of product number 866162.
Z-0011-04	GE Medical Systems Information Technologies	2	Power cord manufactured by ElectriCord Manufacturing Company , P/N 316579, used with DINAMAP Patient Monitors as Follows: DINAMAP PRO Series, DINAMAP PRO 1000 Monitor under both the Critikon and GE Medical Systems. The company name EliectriCord is on the power cord plug.
Z-0042-2015	Mckesson Information Solutions LLC	2	McKesson Cardiology" Hemo intended for complete physiological/hemodynamic monitoring, clinical data acquisition, medical image and data processing, and analytical assessment.
Z-2183-2011	Remote Diagnostic Technologies Ltd. The Old Coach House, The Av. Farleigh Wallop, Basingstoke Hampshire United Kingdom	2	TEMPUS IC PROFESSIONAL Patient Monitor, Part No. 00-1002, Manufactured by: Remote Diagnostics Technologies Ltd., The Old Coach House, Farleigh Wallop, Hants, UK RG25 2HT. Indicated for 3 Lead ECG monitoring and 12 Lead ECG recording, non-invasive blood pressure (NIBP), respiration, end-tidal C02 (ETCO 2), pulse oximetry (SP02) and tympanic temperature.

Similar Registrations

Registration Number	Establishment Name	Location
2133641	BENCHMARK ELECTRONICS, INC.	WINONA, MN, US
3032916632	BECTON, DICKINSON AND COMPANY	Irvine, CA, US
3031823069	AGILEMD	Cupertino, CA, US
3030125003	IMPLICITY	Paris Ile-de-France, FR
3038761440	Corsano Health SA	Plan-les-Ouates Geneve, CH

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3006104191. Last updated year: 2026. Please use registration number 3006104191 when referencing this establishment in official correspondence.