510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K912531Substantially Equivalent

Imd Multicam 1000/2000 Video Camera Systems

Innovative Medical Devices, Inc., Mountain View CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K912531 is the FDA 510(k) clearance record for IMD MULTICAM 1000/2000 VIDEO CAMERA SYSTEMS, a class II device, cleared for Innovative Medical Devices, Inc. on under FDA product code FET (Endoscopic Video Imaging System/Component, Gastroenterology-Urology). FDA's definition for product code FET reads: "To allow for visualization of body cavities through an endoscope by projecting images to a monitor". FDA records list one 510(k) clearance for Innovative Medical Devices, Inc. As of , FDA records show no recalls naming K912531.

Clearance record

Decision date
Received
(89 days to decision)
Product code
FET Endoscopic Video Imaging System/Component, Gastroenterology-Urology
Regulation
21 CFR 876.1500
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
Innovative Medical Devices, Inc. 1637 Grand Rd., Mountain View CA
510(k) summary
Statement
Third party review
No

Clearances, product code FET

Trailing 12 months
3 clearances under product code FET in the twelve months to October 2026, June 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code FET, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20261
July 20261
August 20260
September 20261
October 20260