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FDA 510(k)

KUGEL HERNIA PATCH

K-Number: K963141 · 1996-10-11

ApplicantDouglas Bueschel
Decision Date1996-10-11
Product CodeFTL
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

KUGEL HERNIA PATCH is the device name listed in this FDA 510(k) record. The listed applicant is Douglas Bueschel. It received FDA 510(k) clearance on 1996-10-11 under 510(k) number K963141. The device is classified under product code FTL. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KUGEL HERNIA PATCH?

KUGEL HERNIA PATCH is a medical device that received FDA 510(k) clearance on 1996-10-11. The listed applicant is Douglas Bueschel. The 510(k) number is K963141.

When did KUGEL HERNIA PATCH receive FDA 510(k) clearance?

KUGEL HERNIA PATCH received FDA 510(k) clearance on 1996-10-11, under 510(k) number K963141.

Who is the listed applicant for KUGEL HERNIA PATCH?

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

What is the FDA product code for KUGEL HERNIA PATCH?

The FDA product code for KUGEL HERNIA PATCH is FTL.

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Related Devices (Code: FTL)

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

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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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