QUIK-DOT ANTISTREPTOLYSIN-O
K-Number: K890025 · 1989-01-31
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Device Summary
Frequently Asked Questions
What is the QUIK-DOT ANTISTREPTOLYSIN-O?
QUIK-DOT ANTISTREPTOLYSIN-O is a medical device that received FDA 510(k) clearance on 1989-01-31. The listed applicant is Ampcor, Inc.. The 510(k) number is K890025.
When did QUIK-DOT ANTISTREPTOLYSIN-O receive FDA 510(k) clearance?
QUIK-DOT ANTISTREPTOLYSIN-O received FDA 510(k) clearance on 1989-01-31, under 510(k) number K890025.
Who is the listed applicant for QUIK-DOT ANTISTREPTOLYSIN-O?
The FDA 510(k) record lists Ampcor, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for QUIK-DOT ANTISTREPTOLYSIN-O?
The FDA product code for QUIK-DOT ANTISTREPTOLYSIN-O is GTQ.
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 Ampcor, 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: GTQ)
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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