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FDA 510(k)

UNIVERSAL SWIVEL PATCH

K-Number: K913679 · 1991-09-05

ApplicantBryman Medical
Decision Date1991-09-05
Product CodeKNY
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

UNIVERSAL SWIVEL PATCH is the device name listed in this FDA 510(k) record. The listed applicant is Bryman Medical. It received FDA 510(k) clearance on 1991-09-05 under 510(k) number K913679. The device is classified under product code KNY. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the UNIVERSAL SWIVEL PATCH?

UNIVERSAL SWIVEL PATCH is a medical device that received FDA 510(k) clearance on 1991-09-05. The listed applicant is Bryman Medical. The 510(k) number is K913679.

When did UNIVERSAL SWIVEL PATCH receive FDA 510(k) clearance?

UNIVERSAL SWIVEL PATCH received FDA 510(k) clearance on 1991-09-05, under 510(k) number K913679.

Who is the listed applicant for UNIVERSAL SWIVEL PATCH?

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

What is the FDA product code for UNIVERSAL SWIVEL PATCH?

The FDA product code for UNIVERSAL SWIVEL PATCH is KNY.

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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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