Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K962681Substantially Equivalent

Ecogel 300 TENS Gel

Eco-Med Pharmaceuticals, Inc., Mississauga, Ontario, CA / Traditional, Substantially Equivalent

K962681 is the FDA 510(k) clearance record for ECOGEL 300 TENS GEL, a class II device, cleared for Eco-Med Pharmaceuticals, Inc. on under FDA product code GYB (Media, Electroconductive). FDA records list 4 510(k) clearances for Eco-Med Pharmaceuticals, Inc., from to . As of , FDA records show one recall naming K962681.

Clearance record

Decision date
Received
(86 days to decision)
Product code
GYB Media, Electroconductive
Regulation
21 CFR 882.1275
Device class
Class II
Review panel
Neurology
Applicant
Eco-Med Pharmaceuticals, Inc. 6155 Tomken Rd., Mississauga, Ontario, CA
510(k) summary
Statement
Third party review
No

Clearances, product code GYB

Trailing 12 months

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

FDA records show no clearances under product code GYB in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code GYB, 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