OLYMPUS KD SERIES SPHINCTEROTOME— 510(k) K955247

Substantially Equivalent

Olympus America, Inc.

FDA 510(k) clearance K955247 for OLYMPUS KD SERIES SPHINCTEROTOME, Substantially Equivalent on 1996-04-30. Applicant: Olympus America, Inc..

Clearance details

Applicant: Olympus America, Inc.
Product code: Code KNS
Advisory panel: Gastroenterology, Urology
Date received: 1995-11-15
Decision date: 1996-04-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Melville, NY, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code KNS

product code KNS

Death: 44
Injury: 2,361
Malfunction: 4,771
Total: 7,176

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.