Carapace Debridement Kits

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

510(k) Number

K931669 ↗

FDA Product Code

FRG

Device Class

Class II

Regulation

21 CFR Part 880.6850

Advisory Committee

General Hospital

FDA Decision

SESK Substantially Equivalent — Kit

• Various Disposable Kits/Trays/Instru

  Class I

  FDA 510(k) K840976 Active Cleared 31 May 1984

• Carapace Sterile Cotton Balls

  Class I

  FDA 510(k) K931626 Active Cleared 2 Dec 1993

• Surgical Face Mask

  Class II

  FDA 510(k) K790970 Active Cleared 3 Jul 1979

• Carapace Sterile Gauze Trays

  Class II

  FDA 510(k) K931759 Active Cleared 25 Jan 1994

• Carapace Packing Gauze Trays

  Class II

  FDA 510(k) K931760 Active Cleared 4 Feb 1994

• Carapace Instrumlent and Instrument Sets

  Class II

  FDA 510(k) K931824 Active Cleared 6 Dec 1993

See all devices from Carapace, Inc. →