CBD — Bottle, Collection, Breathing System (Calibrated) Class II

FDA Device Classification

FDA product code CBD covers "Bottle, Collection, Breathing System (Calibrated)", a Class II medical device regulated under 21 CFR 880.6740. Submissions are reviewed by the General Hospital panel. At least 3 recent 510(k) clearances have been granted under this product code.

Classification Details

Product Code
CBD
Device Class
Class II
Regulation Number
880.6740
Submission Type
Review Panel
HO
Medical Specialty
General Hospital
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K780340lkb instrumentsIMV SYSTEMNovember 27, 1978
K770665mcgaw respiratory therapyVALVE, PRESSURE, DEMANDApril 15, 1977
K770369diemoldingVACON TMMarch 1, 1977