510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K000229Substantially Equivalent

Videolabs Medcam Proplus Video Camera and Integral Light Source

Videolabs, Inc., Saint Louis Park MN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K000229 is the FDA 510(k) clearance record for VIDEOLABS MEDCAM PROPLUS VIDEO CAMERA AND INTEGRAL LIGHT SOURCE, a class II device, cleared for Videolabs, Inc. on under FDA product code FCW (Light Source, Fiberoptic, Routine). FDA records list one 510(k) clearance for Videolabs, Inc. As of , FDA records show no recalls naming K000229.

Clearance record

Decision date
Received
(54 days to decision)
Product code
FCW Light Source, Fiberoptic, Routine
Regulation
21 CFR 876.1500
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
Videolabs, Inc. 2530 Pennsylvania Ave., Saint Louis Park MN
510(k) summary
Summary
Third party review
No

Clearances, product code FCW

Trailing 12 months

FDA records hold no clearances under product code FCW in the trailing twelve months.

FDA records show no clearances under product code FCW in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code FCW, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260