K760452

Substantially Equivalent

COLONOSCOPE, 2-CHANNEL LOG (ACMI TX-92)

Applicant: American Cystocope Makers, Inc.
Product code: FDF
Advisory panel: Gastroenterology, Urology
Date received: 1976-08-16
Decision date: 1976-08-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Adverse events under product code FDF

product code FDF

Death: 8
Injury: 729
Malfunction: 61,773
Total: 62,510

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.