LifeSignals, Inc.

FDA Device Registration & Listing · Milpitas, CA, US · Registration 3010552191

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
3010552191
FEI Number
3015191855
Entity Name
LifeSignals, Inc.
City/State/Country
Milpitas, CA, US
Establishment Address
426 South Hillview Drive, Milpitas, CA 95035, US
Establishment Type(s)
Complaint File Establishment per 21 CFR 820.198,Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
LifeSignals, Inc (Owner Number: 10045399)
Owner / Operator Contact Address
426 S. Hillview Drive, Milpitas, CA 95035, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

LifeSignals UbiqVue

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
MWJ Electrocardiograph, Ambulatory (Without Analysis) Cardiovascular Class 2 870.2800 2020-08-01
DRG Transmitters And Receivers, Physiological Signal, Radiofrequency Cardiovascular Class 2 870.2910 2020-08-01

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

LifeSignals, Inc
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
3017446092 LifeSignals India Private Limited Bangalore Karnataka, IN

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K131913 Philips Medizin Systeme Boeblingen GmbH INTELLIVUE CL SPO2 POD AND CL NBP POD, PHILIPS INTELLIVUE PATIENT MONITORS MP5, MP5T, MP5SC 2013-11-26

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3010552191. Last updated year: 2026. Please use registration number 3010552191 when referencing this establishment in official correspondence.
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