Product code KCP— Ear, Nose, Throat

FDA has cleared 4 devices under product code KCP between 1978 and 1984, filed by 4 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.

• 19841 clearance
• 19821 clearance
• 19811 clearance
• 19781 clearance

• R. Wolf Medical Instruments Corp.1 clearance
• Imm Enterprises , Ltd.1 clearance
• American Hospital Supply Corp.1 clearance
• Abco Dealers, Inc.1 clearance

• K840311 — CAT. 7-EAR, NOSE & THROAT DEVICESImm Enterprises , Ltd.·1984-05-09
• K822754 — EAR/ULCER SYRINGEAmerican Hospital Supply Corp.·1982-10-04
• K810284 — AUTOMATIC TEFLON INJECTION SYRINGER. Wolf Medical Instruments Corp.·1981-03-11
• K780599 — SYRINGE, EAR & ULCERAbco Dealers, Inc.·1978-04-19