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FDA 510(k)

HA ANTIGEN

K-Number: K760606 · 1976-10-08

ApplicantFlow Laboratories, Inc.
Decision Date1976-10-08
Product Code
DecisionSubstantially Equivalent

Device Summary

HA ANTIGEN 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 1976-10-08 under 510(k) number K760606. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HA ANTIGEN?

HA ANTIGEN is a medical device that received FDA 510(k) clearance on 1976-10-08. The listed applicant is Flow Laboratories, Inc.. The 510(k) number is K760606.

When did HA ANTIGEN receive FDA 510(k) clearance?

HA ANTIGEN received FDA 510(k) clearance on 1976-10-08, under 510(k) number K760606.

Who is the listed applicant for HA ANTIGEN?

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

Related Clinical Trials

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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.

K861897UNISKAN IIK862066TITERTEK MICROPLATE WASHER S-12K861824GENTAMICIN SULFATE SOLUTION (10MG GENTAMICIN)K861823GENTAMICIN SULFATE SOLUTION (50MG GENTAMICIN)K861791PENICILLIN-STREPTOMYCIN-FUNGIZONEK860762GAMMA-FREE HORSE SERUM

View all 57 devices →

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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