Tecnol Compression Knee Dressing

No FDA recalls on record, checked 11 Oct 2026.

510(k) Number

K873368 ↗

FDA Product Code

LLK

Device Class

Class II

Regulation

21 CFR Part 880.5780

Advisory Committee

General Hospital

FDA Decision

SESE Substantially Equivalent

• Bedpan, Single Patient Use, Tecnol

  Class I

  FDA 510(k) K760307 Active Cleared 11 Aug 1976

• I.V. Support, Tecnol Armboard

  Class I

  FDA 510(k) K760308 Active Cleared 11 Aug 1976

• Tecnol Fog-Free Surgical Mask W/Derma-Touch Tape

  Class II

  FDA 510(k) K873785 Active Cleared 2 Nov 1987

• Tecnol Variable Tension Bandage

  Class I

  FDA 510(k) K884440 Active Cleared 17 Jan 1989

• Tecnol Patient Use Ice Pack

  Class II

  FDA 510(k) K760782 Active Cleared 2 Dec 1976

• Disposable Abdominal Binder

  Class I

  FDA 510(k) K760772 Active Cleared 3 Nov 1976

See all devices from Tecnol New Jersey Wound Care, Inc. →