Bodily Fluid Disposal Kit

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

510(k) Number

K944880 ↗

FDA Product Code

FXX

Device Class

Class II

Regulation

21 CFR Part 878.4040

Advisory Committee

General, Plastic Surgery

FDA Decision

SESE Substantially Equivalent

• Surgical Instruments Kit

  Class II

  FDA 510(k) K941466 Active Cleared 22 Apr 1994

• Skin Scrub Tray

  Class II

  FDA 510(k) K944881 Active Cleared 27 Dec 1994

• Suture Removal Kit

  Class I

  FDA 510(k) K941465 Active Cleared 22 Apr 1994

• Wound Dressing Kit

  Class II

  FDA 510(k) K941467 Active Cleared 12 May 1994

• IV Start Kit

  Class II

  FDA 510(k) K941469 Active Cleared 12 May 1994

• Debridement Tray, Incision and Drainage Tray

  Class II

  FDA 510(k) K941468 Active Cleared 12 May 1994

See all devices from Clinical Resources, Inc. →

• What is the Bodily Fluid Disposal Kit used for?

  The Bodily Fluid Disposal Kit is used for the safe disposal of bodily fluids, providing a comprehensive set of components to handle and dispose of fluids effectively.

• What components are included in the Bodily Fluid Disposal Kit?

  The kit includes various components such as gloves, antimicrobial wipes, absorbent powder, biohazard bags and ties, mask with face shield, and more to ensure safe handling and disposal.

• Is the Bodily Fluid Disposal Kit authorized by regulatory bodies?

  Yes, the Bodily Fluid Disposal Kit has been authorized with an FDA 510K clearance, specifically K944880, indicating its substantial equivalence to existing devices.