510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
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K951695Substantially Equivalent

Operand* Ultrasound Transmission Gel

Redi Products, Inc., Prichard WV / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K951695 is the FDA 510(k) clearance record for OPERAND* ULTRASOUND TRANSMISSION GEL, a class II device, cleared for Redi Products, Inc. on under FDA product code IYN (System, Imaging, Pulsed Doppler, Ultrasonic). FDA records list one 510(k) clearance for Redi Products, Inc. As of , FDA records show no recalls naming K951695.

Clearance record

Decision date
Received
(30 days to decision)
Product code
IYN System, Imaging, Pulsed Doppler, Ultrasonic
Regulation
21 CFR 892.1550
Device class
Class II
Review panel
Radiology
Applicant
Redi Products, Inc. Prichard Industrial Park, Prichard WV
510(k) summary
Summary
Third party review
No

Clearances, product code IYN

Trailing 12 months
55 clearances under product code IYN in the twelve months to October 2026, May 2026 the highest month at 11.
Show the numbers
Monthly 510(k) clearances under FDA product code IYN, trailing twelve months
MonthClearances
November 20256
December 20256
January 20264
February 20261
March 20266
April 20263
May 202611
June 20263
July 20266
August 20263
September 20263
October 20263