ELECTROPHORESIS APPARATUS, FOR CLINICAL USE 160,18— 510(k) K851154

Name: FDA 510(k) clearance K851154
Creator: U.S. Food and Drug Administration
Published: 1985-05-13

Substantially Equivalent

Astral Medical Systems

FDA 510(k) clearance K851154 for ELECTROPHORESIS APPARATUS, FOR CLINICAL USE 160,18, Substantially Equivalent on 1985-05-13. Applicant: Astral Medical Systems. Device class: 1.

Clearance details

Applicant: Astral Medical Systems
Product code: Code JQT
Device class: Class 1
Regulation: 21 CFR 862.2400
Advisory panel: Clinical Chemistry
Date received: 1985-03-22
Decision date: 1985-05-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Buena Park, CA, US

Download summary PDF View on FDA.gov ↗

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