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FDA 510(k)

QUIK-DOT ANTISTREPTOLYSIN-O

K-Number: K890025 · 1989-01-31

ApplicantAmpcor, Inc.
Decision Date1989-01-31
Product CodeGTQ
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

QUIK-DOT ANTISTREPTOLYSIN-O is the device name listed in this FDA 510(k) record. The listed applicant is Ampcor, Inc.. It received FDA 510(k) clearance on 1989-01-31 under 510(k) number K890025. The device is classified under product code GTQ. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 15 devices →

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

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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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