RESPONSIVE RESPIRATORY INC.

FDA Device Registration & Listing · Saint Louis, MO, US · Registration 3005380088

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3005380088
FEI Number
3005380088
Entity Name
RESPONSIVE RESPIRATORY INC.
City/State/Country
Saint Louis, MO, US
Establishment Address
6244 Lemay Ferry Rd, Saint Louis, MO 63129, US
Establishment Type(s)
Repack or Relabel Medical Device
Owner / Operator
RESPONSIVE RESPIRATORY INC. (Owner Number: 9089133)
Owner / Operator Contact Address
6244 Lemay Ferry Rd, --, Saint Louis, MO 63129, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
K061785
PMA Number
N/A

All Registered Proprietary Names

Responsive Respiratory Carry Case Purify O3 View O2 Fingertip PUlse Oximeter Oxygen Tubing - Responsive Respiratory Cylinder, compressed gas, and valve Respond C5 Conserver Oxygen Conserving Device CYL-FIL OXYGEN SYSTEM

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
FOX Stand, Infusion General Hospital Class 1 880.6990 2020-02-25
LRJ Disinfectant, Medical Devices General Hospital Class 1 880.6890 2018-12-14
DQA Oximeter Cardiovascular Class 2 870.2700 2019-11-11
CAT Cannula, Nasal, Oxygen Anesthesiology Class 1 868.5340 2018-12-14
ECX Cylinder, Compressed Gas, And Valve Anesthesiology Class 1 868.2700 2025-02-10
NFB Conserver, Oxygen Anesthesiology Class 2 868.5905 2019-11-11
NFB Conserver, Oxygen Anesthesiology Class 2 868.5905 2025-11-19
BZN Cart, Emergency, Cardiopulmonary (Excluding Equipment) Anesthesiology Class 1 868.6175 2019-11-11
NFB Conserver, Oxygen Anesthesiology Class 2 868.5905 2021-01-25
CAN Regulator, Pressure, Gas Cylinder Anesthesiology Class 1 868.2700 2006-09-05

Official Correspondent

Steven BANNON

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

RESPONSIVE RESPIRATORY INC.
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
K903523 Hewlett-Packard Co. HP MODEL M1020A, ARTERIAL OXYGEN SAT/PLETH MODULE 1990-10-23
K973147 Nellcor Puritan Bennett, Inc. NPB-295 PULSE OXIMETER 1997-11-14
K231243 Guangdong Genial Technology Co., Ltd. Finger Clip Pulse Oximeter 2023-10-31
K971628 Somanetics Corp. SOMANETICS INVOS 3100A CEREBRAL OXIMETER (INVOS) 1997-10-10
K153184 Shenzhen Caremed Medical Technology Co., Ltd. Caremed Reusable & Disposable SPO2 Sensors 2017-01-04

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0020-2019 Oridion Medical 1987 Ltd. Har Hotzvim Industrial 2
CAPNOSTREAM 20 (US) N, Part Number CS08651
Z-0022-2019 Oridion Medical 1987 Ltd. Har Hotzvim Industrial 2
CAPNOSTREAM 20P (US) N - ROHS, Part Number CS08651-02
Z-0023-2019 Oridion Medical 1987 Ltd. Har Hotzvim Industrial 2
CAPNOSTREAM 20P (US) N - ROHS, Part Number CS08651-03
Z-0028-2019 Oridion Medical 1987 Ltd. Har Hotzvim Industrial 2
Capnostream20 (US) M, Part Number CS08653
Z-0029-2019 Oridion Medical 1987 Ltd. Har Hotzvim Industrial 2
Capnostream20 (US) M W/PRINTER, Part Number CS08659

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3005380088. Last updated year: 2026. Please use registration number 3005380088 when referencing this establishment in official correspondence.
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