GENESYS 6000 GAMMA COUNTER— 510(k) K900087

Name: FDA 510(k) clearance K900087
Creator: U.S. Food and Drug Administration
Published: 1990-07-19

Substantially Equivalent

Laboratory Technologies, Inc.

FDA 510(k) clearance K900087 for GENESYS 6000 GAMMA COUNTER, Substantially Equivalent on 1990-07-19. Applicant: Laboratory Technologies, Inc.. Device class: 1.

Clearance details

Applicant: Laboratory Technologies, Inc.
Product code: Code JJJ
Device class: Class 1
Regulation: 21 CFR 862.2320
Advisory panel: Clinical Chemistry
Date received: 1990-01-05
Decision date: 1990-07-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Schaumburg, IL, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.