FDA 510(k) Applications for Medical Device Product Code "BYO"
(Bottle, Blow)

FDA 510(k) Number Applicant Device Name Decision Date
K780558 B & F MEDICAL PRODUCTS, INC. BOTTLE BREATHING DEVICE 05/26/1978
K924541 CONCORD/PORTEX EPIDURAL MINIPACK 07/09/1993
K913527 KIST INTL. HYPERFREE 01/21/1992
K780407 TRAVENOL LABORATORIES, S.A. 2C7125 BLOW BOTTLE 04/10/1978


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