Sterile Pack (Procedural Tray/Kits)

No FDA recalls found in the data synced 22 Oct 2026.

510(k) Number

K882275 ↗

FDA Product Code

LRP

Device Class

Class I

Regulation

21 CFR Part 878.4800

Advisory Committee

General, Plastic Surgery

FDA Decision

SESE Substantially Equivalent

• Towel Pack, Surgical

  Not classified

  FDA 510(k) K863733 Active Cleared 14 Oct 1986

• Nonwoven Surgical Drape Pack

  Class II

  FDA 510(k) K862062 Active Cleared 10 Jun 1986

• Medical, Disposable Bedding

  Class I

  FDA 510(k) K850067 Active Cleared 19 Apr 1985

• Sterilization Wrap Type 22, 44, 77

  Class II

  FDA 510(k) K883376 Active Cleared 28 Sep 1988

• Pad, Pre-Operative Preparation

  Class I

  FDA 510(k) K850811 Active Cleared 21 Mar 1985

• Towel Pack, Surgical

  Not classified

  FDA 510(k) K850016 Active Cleared 23 Jan 1985