MOBILEHELP LLC

FDA Device Registration & Listing · Philadelphia, PA, US · Registration 3008101184

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
3008101184
FEI Number
3008101184
Entity Name
MOBILEHELP LLC
City/State/Country
Philadelphia, PA, US
Establishment Address
1818 Market St, Suite 1200, Philadelphia, PA 19103, US
Establishment Type(s)
Complaint File Establishment per 21 CFR 820.198
Owner / Operator
MobileHelp LLC (Owner Number: 10042590)
Owner / Operator Contact Address
1818 Market St., Suite 1200, Philadelphia, PA 19103, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

Clear Arch Touch Genesis Touch Remote Patient Monitoring System Lifestream Web LifeStream Management Suite Genesis Touch System Clear Arch Classic RPM LifeStream Manager LifeStream Patient Manager LifeStream Clear Arch Mobile Genesis Touch Genesis DM Genesis DM Pro BP

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
OUG Medical Device Data System General Hospital Class 1 880.6310 2015-06-16
DRG Transmitters And Receivers, Physiological Signal, Radiofrequency Cardiovascular Class 2 870.2910 2022-12-05

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

MobileHelp LLC
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
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 3008101184. Last updated year: 2026. Please use registration number 3008101184 when referencing this establishment in official correspondence.
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