TYROSINE 50-HOUR REAGENT KIT
K-Number: K970093 · 1998-03-19
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Device Summary
Frequently Asked Questions
What is the TYROSINE 50-HOUR REAGENT KIT?
TYROSINE 50-HOUR REAGENT KIT is a medical device that received FDA 510(k) clearance on 1998-03-19. The listed applicant is Astoria-Pacific, Inc.. The 510(k) number is K970093.
When did TYROSINE 50-HOUR REAGENT KIT receive FDA 510(k) clearance?
TYROSINE 50-HOUR REAGENT KIT received FDA 510(k) clearance on 1998-03-19, under 510(k) number K970093.
Who is the listed applicant for TYROSINE 50-HOUR REAGENT KIT?
The FDA 510(k) record lists Astoria-Pacific, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TYROSINE 50-HOUR REAGENT KIT?
The FDA product code for TYROSINE 50-HOUR REAGENT KIT is CDR.
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 Astoria-Pacific, 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.
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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