Product code KMO— General Hospital

FDA has cleared 5 devices under product code KMO between 1980 and 1993, filed by 5 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.

• 19931 clearance
• 19892 clearances
• 19881 clearance
• 19801 clearance

• Storer Medical Products1 clearance
• Procter & Gamble Mfg. Co.1 clearance
• General Cardiac Technology, Inc.1 clearance
• Custom Hospitals Products1 clearance
• Boston Pacific Medical, Inc.1 clearance

• K921852 — 4 SURE TM RECTAL TUBEBoston Pacific Medical, Inc.·1993-10-08
• K893809 — COUGH PILLOWCustom Hospitals Products·1989-08-28
• K883214 — THORACIC SUPPORT SYSTEMStorer Medical Products·1989-01-17
• K882592 — HEART HUGGER STERNUM SUPPORT HARNESSGeneral Cardiac Technology, Inc.·1988-09-20
• K792629 — STERILIZATION PROCESS/T-BINDERProcter & Gamble Mfg. Co.·1980-01-11