FDA 510(k) Applications for Medical Device Product Code "CBD"
(Bottle, Collection, Breathing System (Calibrated))

FDA 510(k) Number Applicant Device Name Decision Date
K770369 DIEMOLDING CORP. VACON TM 03/01/1977
K780340 LKB INSTRUMENTS, INC. IMV SYSTEM 11/27/1978
K770665 MCGAW RESPIRATORY THERAPY VALVE, PRESSURE, DEMAND 04/15/1977


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