SYSTEM 6000 AUTOMATED RIA ANALYZER— 510(k) K780886

Name: FDA 510(k) clearance K780886
Creator: U.S. Food and Drug Administration
Published: 1978-09-01

Substantially Equivalent

Beckman Instruments, Inc.

FDA 510(k) clearance K780886 for SYSTEM 6000 AUTOMATED RIA ANALYZER, Substantially Equivalent on 1978-09-01. Applicant: Beckman Instruments, Inc.. Device class: 1.

Clearance details

Applicant: Beckman Instruments, Inc.
Product code: Code LCI
Device class: Class 1
Regulation: 21 CFR 862.2050
Advisory panel: Clinical Chemistry
Date received: 1978-05-26
Decision date: 1978-09-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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