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FDA 510(k)

LifePath Remote Patient Monitoring Platform

K-Number: K211822 · 2022-02-03

ApplicantElastic Care Incorporated
Decision Date2022-02-03
Product CodeDRG
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

LifePath Remote Patient Monitoring Platform is the device name listed in this FDA 510(k) record. The listed applicant is Elastic Care Incorporated. It received FDA 510(k) clearance on 2022-02-03 under 510(k) number K211822. 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 LifePath Remote Patient Monitoring Platform?

LifePath Remote Patient Monitoring Platform is a medical device that received FDA 510(k) clearance on 2022-02-03. The listed applicant is Elastic Care Incorporated. The 510(k) number is K211822.

When did LifePath Remote Patient Monitoring Platform receive FDA 510(k) clearance?

LifePath Remote Patient Monitoring Platform received FDA 510(k) clearance on 2022-02-03, under 510(k) number K211822.

Who is the listed applicant for LifePath Remote Patient Monitoring Platform?

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

What is the FDA product code for LifePath Remote Patient Monitoring Platform?

The FDA product code for LifePath Remote Patient Monitoring Platform is DRG.

Related Clinical Trials

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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.

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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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