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FDA 510(k)

IMPOAID

K-Number: K000730 · 2000-10-19

ApplicantImpoaid, Inc.
Decision Date2000-10-19
Product CodeLKY
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

IMPOAID is the device name listed in this FDA 510(k) record. The listed applicant is Impoaid, Inc.. It received FDA 510(k) clearance on 2000-10-19 under 510(k) number K000730. The device is classified under product code LKY. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IMPOAID?

IMPOAID is a medical device that received FDA 510(k) clearance on 2000-10-19. The listed applicant is Impoaid, Inc.. The 510(k) number is K000730.

When did IMPOAID receive FDA 510(k) clearance?

IMPOAID received FDA 510(k) clearance on 2000-10-19, under 510(k) number K000730.

Who is the listed applicant for IMPOAID?

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

What is the FDA product code for IMPOAID?

The FDA product code for IMPOAID is LKY.

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Related Devices (Code: LKY)

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.

K041573NANMA VACUUM PUMP PROXZEK MODEL 2M9498SNanma Mfg Co., Ltd.K032776VACURECT VACUUM CONSTRICTION DEVICEVacurect Manufacturing (Pty) , Ltd.K030119NANMA ADJUSTABLE CONSTRICTION RINGNanma Mfg Co., Ltd.K030913NANMA VACUUM PUMPNanma Mfg Co., Ltd.K013113MODIFICATION TO NANMA VACUUM PUMPNanma Mfg Co., Ltd.K013051NANMA ADJUSTABLE CONSTRICTION RINGNanma Mfg Co., Ltd.

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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