AUTOMATED ELECTROPHORESIS SYSTEM— 510(k) K780901

Substantially Equivalent

Olympus Corp.

FDA 510(k) clearance K780901 for AUTOMATED ELECTROPHORESIS SYSTEM, Substantially Equivalent on 1978-06-28. Applicant: Olympus Corp.. Device class: 1.

Clearance details

Applicant: Olympus Corp.
Product code: Code JQT
Device class: Class 1
Regulation: 21 CFR 862.2400
Advisory panel: Clinical Chemistry
Date received: 1978-06-01
Decision date: 1978-06-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, 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.