OLYMPUS GF-UM3/EU-M3— 510(k) K882061

Substantially Equivalent

Olympus Corp.

FDA 510(k) clearance K882061 for OLYMPUS GF-UM3/EU-M3, Substantially Equivalent on 1988-11-15. Applicant: Olympus Corp.. Device class: 2.

Clearance details

Applicant: Olympus Corp.
Product code: Code GDB
Device class: Class 2
Regulation: 21 CFR 876.1500
Advisory panel: Gastroenterology, Urology
Date received: 1988-05-16
Decision date: 1988-11-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Lake Success, NY, 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.