Tecnol Patient Use Ice Pack

by Tecnol New Jersey Wound Care, Inc. 510(k)

Active United States

510(k) K760782

Regulatory status

as of 29 Oct 2026

Region	Authorization	Number	Date	Status
United States	FDA 510(k)SESE Substantially Equivalent · Traditional	NumberK760782	Date2 Dec 1976Cleared	StatusActive

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — FDA 510(k) Active

Recalls

0 recalls · FDA

No FDA recalls on record, checked 22 Oct 2026.

Specification

510(k)

510(k) Number: K760782
FDA Product Code: ILO

Device Class: Class II
Regulation: 21 CFR Part 890.5720
Advisory Committee: Physical Medicine
FDA Decision: SESE Substantially Equivalent

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