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FDA 510(k)

BECKMAN LIQUID-STAT AST-UV LIQUID

K-Number: K821433 · 1982-06-02

Decision Date1982-06-02
Product CodeCIT
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

BECKMAN LIQUID-STAT AST-UV LIQUID is the device name listed in this FDA 510(k) record. The listed applicant is Beckman Instruments, Inc.. It received FDA 510(k) clearance on 1982-06-02 under 510(k) number K821433. 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 BECKMAN LIQUID-STAT AST-UV LIQUID?

BECKMAN LIQUID-STAT AST-UV LIQUID is a medical device that received FDA 510(k) clearance on 1982-06-02. The listed applicant is Beckman Instruments, Inc.. The 510(k) number is K821433.

When did BECKMAN LIQUID-STAT AST-UV LIQUID receive FDA 510(k) clearance?

BECKMAN LIQUID-STAT AST-UV LIQUID received FDA 510(k) clearance on 1982-06-02, under 510(k) number K821433.

Who is the listed applicant for BECKMAN LIQUID-STAT AST-UV LIQUID?

The FDA 510(k) record lists Beckman Instruments, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BECKMAN LIQUID-STAT AST-UV LIQUID?

The FDA product code for BECKMAN LIQUID-STAT AST-UV LIQUID 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 Beckman Instruments, 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 281 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

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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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