Product code KPP— Gastroenterology, Urology

FDA has cleared 3 devices under product code KPP between 1980 and 1982, filed by 3 applicant companies. No FDA device recalls reference this product code. Class II devices are moderate-risk and subject to general and special controls; most reach market through 510(k) clearance by demonstrating substantial equivalence to a predicate device.

• 19821 clearance
• 19811 clearance
• 19801 clearance

• Tri-Med, Inc.1 clearance
• Millipore Corp.1 clearance
• Liquid Crystal Products, Inc.1 clearance

• K812615 — TM-CAPDTri-Med, Inc.·1982-01-05
• K803275 — KPP PERITONEAL DIALYSATE FILTERMillipore Corp.·1981-03-13
• K800666 — QUIK-TEMPLiquid Crystal Products, Inc.·1980-05-08