FDA 510(k)

SUPERSLICK

K-Number: K952700 · 1995-10-31

Decision Date1995-10-31

Product CodeJOH

Advisory CommitteeAN

DecisionSubstantially Equivalent

Device Summary

SUPERSLICK is the device name listed in this FDA 510(k) record. The listed applicant is Bivona Medical Technologies. It received FDA 510(k) clearance on 1995-10-31 under 510(k) number K952700. The device is classified under product code JOH. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SUPERSLICK?

SUPERSLICK is a medical device that received FDA 510(k) clearance on 1995-10-31. The listed applicant is Bivona Medical Technologies. The 510(k) number is K952700.

When did SUPERSLICK receive FDA 510(k) clearance?

SUPERSLICK received FDA 510(k) clearance on 1995-10-31, under 510(k) number K952700.

Who is the listed applicant for SUPERSLICK?

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

What is the FDA product code for SUPERSLICK?

The FDA product code for SUPERSLICK is JOH.

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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.