Product code KBC— Ear, Nose, Throat

FDA has cleared 4 devices under product code KBC between 1978 and 1981, 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.

• 19813 clearances
• 19781 clearance

• United States Surgical, A Division of Tyco Healthc2 clearances
• Sierra Laboratories, Inc.1 clearance
• Edward Weck, Inc.1 clearance

• K811887 — SKIN STAPLE EXTRACTORSierra Laboratories, Inc.·1981-07-27
• K810187 — AUTO SUTURE PSS SKIN STAPLING INSTRUMENTUnited States Surgical, A Division of Tyco Healthc·1981-03-20
• K810188 — AUTO SUTURE GAS POWERED DISP. LDS STAPLUnited States Surgical, A Division of Tyco Healthc·1981-03-20
• K772379 — JOSEPH SAWEdward Weck, Inc.·1978-02-02