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FDA 510(k)

WITTMANN PATCH

K-Number: K093166 · 2009-12-07

ApplicantAperta, LLC
Decision Date2009-12-07
Product CodeFTL
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

WITTMANN PATCH is the device name listed in this FDA 510(k) record. The listed applicant is Aperta, LLC. It received FDA 510(k) clearance on 2009-12-07 under 510(k) number K093166. 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 WITTMANN PATCH?

WITTMANN PATCH is a medical device that received FDA 510(k) clearance on 2009-12-07. The listed applicant is Aperta, LLC. The 510(k) number is K093166.

When did WITTMANN PATCH receive FDA 510(k) clearance?

WITTMANN PATCH received FDA 510(k) clearance on 2009-12-07, under 510(k) number K093166.

Who is the listed applicant for WITTMANN PATCH?

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

What is the FDA product code for WITTMANN PATCH?

The FDA product code for WITTMANN 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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