OES LAPARO-THORACO VIDEOSCOPE (RIGID)— 510(k) K955456

Substantially Equivalent

Olympus America, Inc.

FDA 510(k) clearance K955456 for OES LAPARO-THORACO VIDEOSCOPE (RIGID), Substantially Equivalent on 1996-02-22. Applicant: Olympus America, Inc..

Clearance details

Applicant: Olympus America, Inc.
Product code: Code HET
Advisory panel: Obstetrics/Gynecology
Date received: 1995-11-29
Decision date: 1996-02-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Melville, NY, US

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Adverse events under product code HET

product code HET

Malfunction: 10,504
Total: 10,504

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

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