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FDA 510(k)

TYROSINE 50-HOUR REAGENT KIT

K-Number: K970093 · 1998-03-19

Decision Date1998-03-19
Product CodeCDR
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

TYROSINE 50-HOUR REAGENT KIT is the device name listed in this FDA 510(k) record. The listed applicant is Astoria-Pacific, Inc.. It received FDA 510(k) clearance on 1998-03-19 under 510(k) number K970093. The device is classified under product code CDR. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

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.

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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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