BINAX STREP A TEST
K-Number: K960712 · 1996-03-22
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Device Summary
Frequently Asked Questions
What is the BINAX STREP A TEST?
BINAX STREP A TEST is a medical device that received FDA 510(k) clearance on 1996-03-22. The listed applicant is Binax, Inc.. The 510(k) number is K960712.
When did BINAX STREP A TEST receive FDA 510(k) clearance?
BINAX STREP A TEST received FDA 510(k) clearance on 1996-03-22, under 510(k) number K960712.
Who is the listed applicant for BINAX STREP A TEST?
The FDA 510(k) record lists Binax, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BINAX STREP A TEST?
The FDA product code for BINAX STREP A TEST is GTZ.
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 Binax, 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: GTZ)
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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