FDA 510(k)

CONVERTORS STERILIZATION WRAP

K-Number: K921243 · 1992-10-28

Decision Date1992-10-28

Product CodeFRG

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

CONVERTORS STERILIZATION WRAP is the device name listed in this FDA 510(k) record. The listed applicant is Baxter Healthcare Corp. It received FDA 510(k) clearance on 1992-10-28 under 510(k) number K921243. The device is classified under product code FRG. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CONVERTORS STERILIZATION WRAP?

CONVERTORS STERILIZATION WRAP is a medical device that received FDA 510(k) clearance on 1992-10-28. The listed applicant is Baxter Healthcare Corp. The 510(k) number is K921243.

When did CONVERTORS STERILIZATION WRAP receive FDA 510(k) clearance?

CONVERTORS STERILIZATION WRAP received FDA 510(k) clearance on 1992-10-28, under 510(k) number K921243.

Who is the listed applicant for CONVERTORS STERILIZATION WRAP?

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

What is the FDA product code for CONVERTORS STERILIZATION WRAP?

The FDA product code for CONVERTORS STERILIZATION WRAP is FRG.

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Related Devices (Code: FRG)

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.