VIDEOLABS MEDCAM PROPLUS VIDEO CAMERA AND INTEGRAL LIGHT SOURCE— 510(k) K000229

Substantially Equivalent

Videolabs, Inc.

FDA 510(k) clearance K000229 for VIDEOLABS MEDCAM PROPLUS VIDEO CAMERA AND INTEGRAL LIGHT SOURCE, Substantially Equivalent on 2000-03-21. Applicant: Videolabs, Inc..

Clearance details

Applicant: Videolabs, Inc.
Product code: Code FCW
Advisory panel: Gastroenterology, Urology
Date received: 2000-01-27
Decision date: 2000-03-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Saint Louis Park, MN, US

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Adverse events under product code FCW

product code FCW

Malfunction: 912
Other: 1
Total: 913

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.