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FDA 510(k)

DISPOSABLE FLUID COLLECTION BAG

K-Number: K904133 · 1990-10-11

Decision Date1990-10-11
Product CodeGBX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

DISPOSABLE FLUID COLLECTION BAG is the device name listed in this FDA 510(k) record. The listed applicant is Axiom Medical, Inc.. It received FDA 510(k) clearance on 1990-10-11 under 510(k) number K904133. The device is classified under product code GBX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DISPOSABLE FLUID COLLECTION BAG?

DISPOSABLE FLUID COLLECTION BAG is a medical device that received FDA 510(k) clearance on 1990-10-11. The listed applicant is Axiom Medical, Inc.. The 510(k) number is K904133.

When did DISPOSABLE FLUID COLLECTION BAG receive FDA 510(k) clearance?

DISPOSABLE FLUID COLLECTION BAG received FDA 510(k) clearance on 1990-10-11, under 510(k) number K904133.

Who is the listed applicant for DISPOSABLE FLUID COLLECTION BAG?

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

What is the FDA product code for DISPOSABLE FLUID COLLECTION BAG?

The FDA product code for DISPOSABLE FLUID COLLECTION BAG is GBX.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Axiom Medical, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 28 devices →

Related Devices (Code: GBX)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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