FDA 510(k)

STETSKINS

K-Number: K930118 · 1993-03-26

Decision Date1993-03-26

Product CodeBZS

Advisory CommitteeAN

DecisionSubstantially Equivalent

Device Summary

STETSKINS is the device name listed in this FDA 510(k) record. The listed applicant is Nova Diversified Concepts. It received FDA 510(k) clearance on 1993-03-26 under 510(k) number K930118. The device is classified under product code BZS. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STETSKINS?

STETSKINS is a medical device that received FDA 510(k) clearance on 1993-03-26. The listed applicant is Nova Diversified Concepts. The 510(k) number is K930118.

When did STETSKINS receive FDA 510(k) clearance?

STETSKINS received FDA 510(k) clearance on 1993-03-26, under 510(k) number K930118.

Who is the listed applicant for STETSKINS?

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

What is the FDA product code for STETSKINS?

The FDA product code for STETSKINS is BZS.

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Related Devices (Code: BZS)

K935146DISPOSABLE STETHOSCOPE HEAD COVERModern Medical Devices, Inc.K801050SUPRA SCOPEWarner-Lambert Co.

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.