AUTOMATED ELECTROPHORESES MACHINE— 510(k) K791111

Name: FDA 510(k) clearance K791111
Creator: U.S. Food and Drug Administration
Published: 1979-07-30

Substantially Equivalent

Gelman Sciences, Inc.

FDA 510(k) clearance K791111 for AUTOMATED ELECTROPHORESES MACHINE, Substantially Equivalent on 1979-07-30. Applicant: Gelman Sciences, Inc.. Device class: 1.

Clearance details

Applicant: Gelman Sciences, Inc.
Product code: Code JJN
Device class: Class 1
Regulation: 21 CFR 862.2485
Advisory panel: Clinical Chemistry
Date received: 1979-06-14
Decision date: 1979-07-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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