FDA 510(k) Applications for Medical Device Product Code "CAO"
(Airway, Esophageal (Obturator))

FDA 510(k) Number Applicant Device Name Decision Date
K864200 CRANCO CO. VETA/VENTED ESOPHAGEAL TUBE AIRWAY 03/17/1987
K971348 GREEN FIELD MEDICAL SOURCING, INC. FASTTRACH SINGLE-PASS TRACHEAL/ESOPHAGEAL AIRWAY SYSTEM 02/27/1998
K761195 MCKESSON CORP. ESOPHAGEAL OBTURATION AIRWAY 12/09/1976
K863172 RESPIRONICS, INC. RESPIRONICS PTL REVIVEEASY 11/04/1986
K894032 SHARN, INC. EVAC-TUBE 08/31/1989
K875226 SHERIDAN CATHETER CORP. ESOPHAGEAL OBTURATOR/TRACHEAL TUBE 01/19/1988


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