INFLUENZA HA ANTIGEN A/USSR
K-Number: K780275 · 1978-02-28
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Device Summary
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.
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
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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