Product code CAM— Anesthesiology

FDA has cleared 8 devices under product code CAM between 1977 and 1994, 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.

• 19941 clearance
• 19854 clearances
• 19841 clearance
• 19781 clearance
• 19771 clearance

• Penox Technologies, Inc.4 clearances
• Spica, Inc.1 clearance
• Siemens Elema AB1 clearance
• Bel-Med, Inc.1 clearance
• American Gage & Medical, Inc.1 clearance

• K935283 — YOKE ASSEMBLY MEDICAL GASAmerican Gage & Medical, Inc.·1994-03-11
• K851215 — T-HANDLE ADAPTER, U-HANDLE & L HANDLER ADAPTERPenox Technologies, Inc.·1985-06-18
• K851216 — PENOX DUAL FEED MANIFOLDPenox Technologies, Inc.·1985-06-18
• K851217 — PENOX DUAL FLOW MINIFOLDPenox Technologies, Inc.·1985-06-18
• K851219 — FILL HOSE SAFETY ADAPTERPenox Technologies, Inc.·1985-06-18
• K840326 — GAS SUPPLY MANIFOLD SIEMENS-ELEMA ABSiemens Elema AB·1984-06-07
• K780365 — OXYGEN/NITROUS OXIDE OUTLETSpica, Inc.·1978-03-30
• K770426 — OXYGEN MANIFOLD SYSTEMS, NITROUS OXIDEBel-Med, Inc.·1977-03-15