Product code KBG— Ear, Nose, Throat

FDA has cleared 3 devices under product code KBG between 1985 and 2005, filed by 3 applicant companies. No FDA device recalls reference this product code. Class I devices are low-risk and subject to FDA general controls; many Class I device types are exempt from 510(k) premarket notification.

• 20051 clearance
• 20021 clearance
• 19851 clearance

• Clearmedical, Inc.1 clearance
• Chesebrough-Pond'S U.S.A. Co.1 clearance
• Adven Medical1 clearance

• K033591 — REPROCESSED TROCARSClearmedical, Inc.·2005-06-03
• K013987 — REPROCESSED DISPOSABLE TROCARSAdven Medical·2002-03-01
• K844186 — CONTINENT STOMA SYSTEM & ACCESSORIESChesebrough-Pond'S U.S.A. Co.·1985-01-15