KEY-MED FIBRESCOPE DISINFECTION TROLLEY— 510(k) K810818

Substantially Equivalent

Keymed, Inc.

FDA 510(k) clearance K810818 for KEY-MED FIBRESCOPE DISINFECTION TROLLEY, Substantially Equivalent on 1981-04-08. Applicant: Keymed, Inc..

Clearance details

Applicant: Keymed, Inc.
Product code: Code FEB
Advisory panel: Gastroenterology, Urology
Date received: 1981-03-24
Decision date: 1981-04-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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Adverse events under product code FEB

product code FEB

Malfunction: 3,879
Total: 3,879

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.