FISHER DIAGNOSTIC LATEST ASO TEST KIT
K-Number: K852701 · 1985-07-19
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Device Summary
Frequently Asked Questions
What is the FISHER DIAGNOSTIC LATEST ASO TEST KIT?
FISHER DIAGNOSTIC LATEST ASO TEST KIT is a medical device that received FDA 510(k) clearance on 1985-07-19. The listed applicant is Allied Fisher Scientific. The 510(k) number is K852701.
When did FISHER DIAGNOSTIC LATEST ASO TEST KIT receive FDA 510(k) clearance?
FISHER DIAGNOSTIC LATEST ASO TEST KIT received FDA 510(k) clearance on 1985-07-19, under 510(k) number K852701.
Who is the listed applicant for FISHER DIAGNOSTIC LATEST ASO TEST KIT?
The FDA 510(k) record lists Allied Fisher Scientific as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for FISHER DIAGNOSTIC LATEST ASO TEST KIT?
The FDA product code for FISHER DIAGNOSTIC LATEST ASO TEST KIT 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.
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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