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FDA 510(k)

RESQPOD CIRCULATORY ENHANCER

K-Number: K022906 · 2003-06-11

ApplicantCprx, LLC
Decision Date2003-06-11
Product CodeBWF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

RESQPOD CIRCULATORY ENHANCER is the device name listed in this FDA 510(k) record. The listed applicant is Cprx, LLC. It received FDA 510(k) clearance on 2003-06-11 under 510(k) number K022906. The device is classified under product code BWF. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RESQPOD CIRCULATORY ENHANCER?

RESQPOD CIRCULATORY ENHANCER is a medical device that received FDA 510(k) clearance on 2003-06-11. The listed applicant is Cprx, LLC. The 510(k) number is K022906.

When did RESQPOD CIRCULATORY ENHANCER receive FDA 510(k) clearance?

RESQPOD CIRCULATORY ENHANCER received FDA 510(k) clearance on 2003-06-11, under 510(k) number K022906.

Who is the listed applicant for RESQPOD CIRCULATORY ENHANCER?

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

What is the FDA product code for RESQPOD CIRCULATORY ENHANCER?

The FDA product code for RESQPOD CIRCULATORY ENHANCER is BWF.

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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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