510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K760782Substantially Equivalent

Tecnol Patient Use Ice Pack

Tecnol New Jersey Wound Care, Inc., Hammonton NJ / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K760782 is the FDA 510(k) clearance record for TECNOL PATIENT USE ICE PACK, a class II device, cleared for Tecnol New Jersey Wound Care, Inc. on under FDA product code ILO (Pack, Hot Or Cold, Water Circulating). FDA records list 35 510(k) clearances for Tecnol New Jersey Wound Care, Inc., from to . As of , FDA records show no recalls naming K760782.

Clearance record

Decision date
Received
(58 days to decision)
Product code
ILO Pack, Hot Or Cold, Water Circulating
Regulation
21 CFR 890.5720
Device class
Class II
Review panel
Physical Medicine
Applicant
Tecnol New Jersey Wound Care, Inc. 368 Fairview Ave., Hammonton NJ
Third party review
No

Clearances, product code ILO

Trailing 12 months

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

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