FDA 510(k)

PREVEN-A-STIK

K-Number: K904148 · 1990-11-21

Decision Date1990-11-21

Product CodeMMK

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

PREVEN-A-STIK is the device name listed in this FDA 510(k) record. The listed applicant is Preven-A-Stik, Inc.. It received FDA 510(k) clearance on 1990-11-21 under 510(k) number K904148. The device is classified under product code MMK. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PREVEN-A-STIK?

PREVEN-A-STIK is a medical device that received FDA 510(k) clearance on 1990-11-21. The listed applicant is Preven-A-Stik, Inc.. The 510(k) number is K904148.

When did PREVEN-A-STIK receive FDA 510(k) clearance?

PREVEN-A-STIK received FDA 510(k) clearance on 1990-11-21, under 510(k) number K904148.

Who is the listed applicant for PREVEN-A-STIK?

The FDA 510(k) record lists Preven-A-Stik, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PREVEN-A-STIK?

The FDA product code for PREVEN-A-STIK is MMK.

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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.