Product code BSF— Anesthesiology

FDA has cleared 8 devices under product code BSF between 1976 and 1995, filed by 7 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.

• 19951 clearance
• 19851 clearance
• 19842 clearances
• 19831 clearance
• 19821 clearance
• 19801 clearance
• 19761 clearance

• Ohmeda Medical2 clearances
• Penlon, Inc.1 clearance
• Ohio Medical Products1 clearance
• King Systems Corp.1 clearance
• G & L Unltd.1 clearance
• Fraser Sweatman, Inc.1 clearance
• Airco/Ohio Medical Products1 clearance

• K951093 — KAB SYSTEMKing Systems Corp.·1995-03-24
• K852071 — OHMEDA GMS ABOSORBEROhmeda Medical·1985-07-15
• K843422 — OHMEDA BAIN CIRCUIT ADAPTER GMS ABSOROhmeda Medical·1984-10-23
• K834535 — NITROUS OXIDE RECYCLERG & L Unltd.·1984-06-07
• K833452 — OHIO GMS ABSORBERAirco/Ohio Medical Products·1983-11-29
• K821144 — OHIO ABSORBEROhio Medical Products·1982-05-28
• K801255 — PENLON JUMBO CARBON DIOXIDE ABSORBERPenlon, Inc.·1980-06-04
• K760076 — ABSORBER, ANESTHESIA CIRCLE SYS, CO2Fraser Sweatman, Inc.·1976-07-16