BECKMAN LIQUID-STAT AST-UV LIQUID
K-Number: K821433 · 1982-06-02
Advertisement
Device Summary
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.
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.
Advertisement