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FDA 510(k)

ALLEGIANCE GENESIS CONTAINER SYSTEM

K-Number: K983299 · 2000-08-04

ApplicantAllegiance Healthcare Corp.
Decision Date2000-08-04
Product CodeFRG
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

ALLEGIANCE GENESIS 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 2000-08-04 under 510(k) number K983299. 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 ALLEGIANCE GENESIS CONTAINER SYSTEM?

ALLEGIANCE GENESIS CONTAINER SYSTEM is a medical device that received FDA 510(k) clearance on 2000-08-04. The listed applicant is Allegiance Healthcare Corp.. The 510(k) number is K983299.

When did ALLEGIANCE GENESIS CONTAINER SYSTEM receive FDA 510(k) clearance?

ALLEGIANCE GENESIS CONTAINER SYSTEM received FDA 510(k) clearance on 2000-08-04, under 510(k) number K983299.

Who is the listed applicant for ALLEGIANCE GENESIS 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 ALLEGIANCE GENESIS CONTAINER SYSTEM?

The FDA product code for ALLEGIANCE GENESIS 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.

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