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FDA 510(k)

THE POUCH GROIN & ABDOMINAL STRESS AID

K-Number: K892379 · 1989-07-20

ApplicantKuhn Industries
Decision Date1989-07-20
Product CodeFSD
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

THE POUCH GROIN & ABDOMINAL STRESS AID is the device name listed in this FDA 510(k) record. The listed applicant is Kuhn Industries. It received FDA 510(k) clearance on 1989-07-20 under 510(k) number K892379. The device is classified under product code FSD. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THE POUCH GROIN & ABDOMINAL STRESS AID?

THE POUCH GROIN & ABDOMINAL STRESS AID is a medical device that received FDA 510(k) clearance on 1989-07-20. The listed applicant is Kuhn Industries. The 510(k) number is K892379.

When did THE POUCH GROIN & ABDOMINAL STRESS AID receive FDA 510(k) clearance?

THE POUCH GROIN & ABDOMINAL STRESS AID received FDA 510(k) clearance on 1989-07-20, under 510(k) number K892379.

Who is the listed applicant for THE POUCH GROIN & ABDOMINAL STRESS AID?

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

What is the FDA product code for THE POUCH GROIN & ABDOMINAL STRESS AID?

The FDA product code for THE POUCH GROIN & ABDOMINAL STRESS AID is FSD.

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Related Devices (Code: FSD)

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.

K822817DOCE ALL-IN-THE-EAR AIDFidelty Hearing Instruments, Inc.K810379EARETTE HEARING AID SEARS #8054Oticon Corp.K770162MATERNITY SUPPORTERR.G. MooreK760772DISPOSABLE ABDOMINAL BINDERTecnol New Jersey Wound Care, Inc.

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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