FDA 510(k)

GENESIS STERRAD COMPATIBLE REUSABLE STERILIZATION CONTAINER SYSTEM

K-Number: K012931 · 2002-08-20

Decision Date2002-08-20

Product CodeFRG

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

GENESIS STERRAD COMPATIBLE REUSABLE STERILIZATION CONTAINER SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Allegiance Healthcare Corp.. It received FDA 510(k) clearance on 2002-08-20 under 510(k) number K012931. 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 GENESIS STERRAD COMPATIBLE REUSABLE STERILIZATION CONTAINER SYSTEM?

GENESIS STERRAD COMPATIBLE REUSABLE STERILIZATION CONTAINER SYSTEM is a medical device that received FDA 510(k) clearance on 2002-08-20. The listed applicant is Allegiance Healthcare Corp.. The 510(k) number is K012931.

When did GENESIS STERRAD COMPATIBLE REUSABLE STERILIZATION CONTAINER SYSTEM receive FDA 510(k) clearance?

GENESIS STERRAD COMPATIBLE REUSABLE STERILIZATION CONTAINER SYSTEM received FDA 510(k) clearance on 2002-08-20, under 510(k) number K012931.

Who is the listed applicant for GENESIS STERRAD COMPATIBLE REUSABLE STERILIZATION CONTAINER SYSTEM?

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

What is the FDA product code for GENESIS STERRAD COMPATIBLE REUSABLE STERILIZATION CONTAINER SYSTEM?

The FDA product code for GENESIS STERRAD COMPATIBLE REUSABLE STERILIZATION CONTAINER SYSTEM is FRG.

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Other records listing Allegiance Healthcare Corp. as applicant

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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.