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FDA 510(k)

WIENER LAB GOT (AST) UV AA LIQUIDA

K-Number: K023551 · 2002-12-09

Decision Date2002-12-09
Product CodeCIT
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

WIENER LAB GOT (AST) UV AA LIQUIDA is the device name listed in this FDA 510(k) record. The listed applicant is Wiener Laboratories Saic. It received FDA 510(k) clearance on 2002-12-09 under 510(k) number K023551. The device is classified under product code CIT. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WIENER LAB GOT (AST) UV AA LIQUIDA?

WIENER LAB GOT (AST) UV AA LIQUIDA is a medical device that received FDA 510(k) clearance on 2002-12-09. The listed applicant is Wiener Laboratories Saic. The 510(k) number is K023551.

When did WIENER LAB GOT (AST) UV AA LIQUIDA receive FDA 510(k) clearance?

WIENER LAB GOT (AST) UV AA LIQUIDA received FDA 510(k) clearance on 2002-12-09, under 510(k) number K023551.

Who is the listed applicant for WIENER LAB GOT (AST) UV AA LIQUIDA?

The FDA 510(k) record lists Wiener Laboratories Saic as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for WIENER LAB GOT (AST) UV AA LIQUIDA?

The FDA product code for WIENER LAB GOT (AST) UV AA LIQUIDA is CIT.

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 Wiener Laboratories Saic 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 24 devices →

Related Devices (Code: CIT)

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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