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FDA 510(k)

INFLUENZA HA ANTIGEN A/USSR

K-Number: K780275 · 1978-02-28

Decision Date1978-02-28
Product CodeGNT
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

INFLUENZA HA ANTIGEN A/USSR is the device name listed in this FDA 510(k) record. The listed applicant is Flow Laboratories, Inc.. It received FDA 510(k) clearance on 1978-02-28 under 510(k) number K780275. The device is classified under product code GNT. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INFLUENZA HA ANTIGEN A/USSR?

INFLUENZA HA ANTIGEN A/USSR is a medical device that received FDA 510(k) clearance on 1978-02-28. The listed applicant is Flow Laboratories, Inc.. The 510(k) number is K780275.

When did INFLUENZA HA ANTIGEN A/USSR receive FDA 510(k) clearance?

INFLUENZA HA ANTIGEN A/USSR received FDA 510(k) clearance on 1978-02-28, under 510(k) number K780275.

Who is the listed applicant for INFLUENZA HA ANTIGEN A/USSR?

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

What is the FDA product code for INFLUENZA HA ANTIGEN A/USSR?

The FDA product code for INFLUENZA HA ANTIGEN A/USSR is GNT.

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 Flow Laboratories, 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 57 devices →

Related Devices (Code: GNT)

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

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

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