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FDA 510(k)

RHYTHM OF LIFE, MODEL R0901-05

K-Number: K092408 · 2009-10-14

ApplicantRapid Response Solutions, LLC
Decision Date2009-10-14
Product CodeLIX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

RHYTHM OF LIFE, MODEL R0901-05 is the device name listed in this FDA 510(k) record. The listed applicant is Rapid Response Solutions, LLC. It received FDA 510(k) clearance on 2009-10-14 under 510(k) number K092408. The device is classified under product code LIX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RHYTHM OF LIFE, MODEL R0901-05?

RHYTHM OF LIFE, MODEL R0901-05 is a medical device that received FDA 510(k) clearance on 2009-10-14. The listed applicant is Rapid Response Solutions, LLC. The 510(k) number is K092408.

When did RHYTHM OF LIFE, MODEL R0901-05 receive FDA 510(k) clearance?

RHYTHM OF LIFE, MODEL R0901-05 received FDA 510(k) clearance on 2009-10-14, under 510(k) number K092408.

Who is the listed applicant for RHYTHM OF LIFE, MODEL R0901-05?

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

What is the FDA product code for RHYTHM OF LIFE, MODEL R0901-05?

The FDA product code for RHYTHM OF LIFE, MODEL R0901-05 is LIX.

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Official Source

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

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