FIBER OPTIC ENDOSCOPE— 510(k) K921918

Substantially Equivalent

Electro Fiberoptics Corp.

FDA 510(k) clearance K921918 for FIBER OPTIC ENDOSCOPE, Substantially Equivalent on 1993-08-17. Applicant: Electro Fiberoptics Corp..

Clearance details

Applicant: Electro Fiberoptics Corp.
Product code: Code GCM
Advisory panel: Gastroenterology, Urology
Date received: 1992-04-23
Decision date: 1993-08-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Northborough, MA, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code GCM

product code GCM

Malfunction: 1,233
Total: 1,233

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.