Thermal Option

No FDA recalls found in the data synced 10 Oct 2026.

510(k) Number

K932790 ↗

FDA Product Code

KGE

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

• Cox Disposable Polypectomy Snares

  Class II

  FDA 510(k) K923671 Active Cleared 13 Oct 1992

• Basics Endoscopy System

  Class II

  FDA 510(k) K940911 Active Cleared 16 May 1994

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