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BYO — Bottle, Blow Class I

FDA Device Classification

Classification Details

Product Code
BYO
Device Class
Class I
Regulation Number
868.5220
Submission Type
Review Panel
AN
Medical Specialty
Anesthesiology
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K924541concord/portexEPIDURAL MINIPACKJuly 9, 1993
K913527kist intlHYPERFREEJanuary 21, 1992
K780558b and f medical productsBOTTLE BREATHING DEVICEMay 26, 1978
K780407travenol laboratories2C7125 BLOW BOTTLEApril 10, 1978