CAM — Yoke Assembly, Medical Gas Class I

FDA Device Classification

FDA product code CAM covers "Yoke Assembly, Medical Gas", a Class I medical device regulated under 21 CFR 868.6885. Submissions are reviewed by the Anesthesiology panel. At least 8 recent 510(k) clearances have been granted under this product code.

Classification Details

Product Code
CAM
Device Class
Class I
Regulation Number
868.6885
Submission Type
Review Panel
AN
Medical Specialty
Anesthesiology
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K935283american gage and medicalYOKE ASSEMBLY MEDICAL GASMarch 11, 1994
K851216penox technologiesPENOX DUAL FEED MANIFOLDJune 18, 1985
K851217penox technologiesPENOX DUAL FLOW MINIFOLDJune 18, 1985
K851215penox technologiesT-HANDLE ADAPTER, U-HANDLE & L HANDLER ADAPTERJune 18, 1985
K851219penox technologiesFILL HOSE SAFETY ADAPTERJune 18, 1985
K840326siemens elemaGAS SUPPLY MANIFOLD SIEMENS-ELEMA ABJune 7, 1984
K780365spicaOXYGEN/NITROUS OXIDE OUTLETMarch 30, 1978
K770426bel-medOXYGEN MANIFOLD SYSTEMS, NITROUS OXIDEMarch 15, 1977