510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K963274Substantially Equivalent

V-Link 3.2 for Windows

Koven Technology, Inc., St. Louis MO / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K963274 is the FDA 510(k) clearance record for V-LINK 3.2 FOR WINDOWS, a class II device, cleared for Koven Technology, Inc. on under FDA product code IYO (System, Imaging, Pulsed Echo, Ultrasonic). FDA records list 18 510(k) clearances for Koven Technology, Inc., from to . As of , FDA records show no recalls naming K963274.

Clearance record

Decision date
Received
(72 days to decision)
Product code
IYO System, Imaging, Pulsed Echo, Ultrasonic
Regulation
21 CFR 892.1560
Device class
Class II
Review panel
Radiology
Applicant
Koven Technology, Inc. 300 Brookes Dr., St. Louis MO
510(k) summary
Statement
Third party review
No

Clearances, product code IYO

Trailing 12 months
8 clearances under product code IYO in the twelve months to October 2026, February 2026 the highest month at 2.
Show the numbers
Monthly 510(k) clearances under FDA product code IYO, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20262
March 20261
April 20262
May 20260
June 20261
July 20261
August 20260
September 20261
October 20260