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FDA 510(k)

CONSTANT CARE LILAH HOME HEALTH MONITORING SYSTEM

K-Number: K120941 · 2012-07-03

ApplicantConstant Care, LLC
Decision Date2012-07-03
Product CodeDRG
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CONSTANT CARE LILAH HOME HEALTH MONITORING SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Constant Care, LLC. It received FDA 510(k) clearance on 2012-07-03 under 510(k) number K120941. The device is classified under product code DRG. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CONSTANT CARE LILAH HOME HEALTH MONITORING SYSTEM?

CONSTANT CARE LILAH HOME HEALTH MONITORING SYSTEM is a medical device that received FDA 510(k) clearance on 2012-07-03. The listed applicant is Constant Care, LLC. The 510(k) number is K120941.

When did CONSTANT CARE LILAH HOME HEALTH MONITORING SYSTEM receive FDA 510(k) clearance?

CONSTANT CARE LILAH HOME HEALTH MONITORING SYSTEM received FDA 510(k) clearance on 2012-07-03, under 510(k) number K120941.

Who is the listed applicant for CONSTANT CARE LILAH HOME HEALTH MONITORING SYSTEM?

The FDA 510(k) record lists Constant Care, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CONSTANT CARE LILAH HOME HEALTH MONITORING SYSTEM?

The FDA product code for CONSTANT CARE LILAH HOME HEALTH MONITORING SYSTEM is DRG.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Other records listing Constant Care, LLC as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K130360CONSTANT CARE LILAH HOME HEALTH MONITORING SYSTEM - MULTI-USER VERSION

Related Devices (Code: DRG)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K261569UbiqVue™ 2AYe Cardiac System (UX2253)Lifesignals, Inc.K252984Perin Health System (PHD80060-2)Perin Health Devices, LLCK252440EasyTeleMed (2.0.2)Ingeniars S.R.L.K250259TeleRehab Aermos Cardiopulmonary RehabilitationThe ScottCare CorporationK243837iBSMIorbit Digital Technologies Private LimitedK242018UbiqVue™ 2A Multi-parameter System (UX2550)Lifesignals, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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