Surgical Instrument Kit, Disposable

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K920989 ↗

FDA Product Code

KDD

Device Class

Class I

Regulation

21 CFR Part 878.4800

Advisory Committee

General, Plastic Surgery

FDA Decision

SEKD

• Absorbent Fiber

  Class I

  FDA 510(k) K914431 Active Cleared 4 Dec 1991

• Ulcer Wound Tray

  Class II

  FDA 510(k) K922828 Active Cleared 28 Sep 1992

• Absorbable Gauze Drape

  Class II

  FDA 510(k) K901465 Active Cleared 12 Jun 1990

• Ulticare Safety Insulin Syringe

  Class II

  FDA 510(k) K103011 Active Cleared 2 Feb 2011

• Post Operative Sponge

  Class I

  FDA 510(k) K912693 Active Cleared 4 Oct 1991

• Cover, Shoe Operating Room

  Class I

  FDA 510(k) K865023 Active Cleared 12 Jan 1987

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