Cox Disposable Polypectomy Snares

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

510(k) Number

K923671 ↗

FDA Product Code

FDI

Device Class

Class II

Regulation

21 CFR Part 876.4300

Advisory Committee

Gastroenterology, Urology

FDA Decision

SESE Substantially Equivalent

• Cox Disposable Cytology Brushes

  Class II

  FDA 510(k) K914466 Active Cleared 25 Oct 1991

• Modular Biopsy Forcep

  Class I

  FDA 510(k) K946360 Active Cleared 6 Mar 1995

• Cox Diaposable Polypectomy Snare

  Class II

  FDA 510(k) K912254 Active Cleared 26 Jul 1991

• Cox Disposable Endoscope Cleaning Brush(Cb-X2)

  Class II

  FDA 510(k) K924655 Active Cleared 15 Dec 1992

• Basics Endoscopy System

  Class II

  FDA 510(k) K940911 Active Cleared 16 May 1994

• Cox Disposable Endoscope Cleaning Brush

  Class II

  FDA 510(k) K914442 Active Cleared 25 Oct 1991

See all devices from Cox Medical Ent., Inc. →

• What clinical procedures are these snares intended for?

  The Cox Disposable Polypectomy Snares are designed for polypectomy during endoscopic procedures in both gastroenterology and urology, allowing clinicians to capture and excise polyps safely within the gastrointestinal or urinary tracts.

• Are the snares supplied as sterile, single‑use items?

  Yes, the snares are provided as disposable, single‑use devices. This eliminates the need for re‑processing, reduces cross‑contamination risk, and ensures consistent performance for each procedure.

• How are these devices classified and regulated?

  They are classified as Class II medical devices under regulation 876.4300 and received traditional FDA 510(k) clearance (K923671) on October 13 1992, indicating they are substantially equivalent to a legally marketed predicate device.

• What material flexibility does the snare offer during polyp removal?

  The snares are described as flexible, which helps the operator maneuver the loop around polyps of varying shapes and locations, improving capture efficiency while minimizing trauma to surrounding tissue.