BYW — Device, Rebreathing Class I

FDA Device Classification

Classification Details

Product Code
BYW
Device Class
Class I
Regulation Number
868.5675
Submission Type
Review Panel
AN
Medical Specialty
Anesthesiology
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K895274global businessHYPEXFebruary 23, 1990
K802165sherwood medicalSHERWOOD VENTILATORY MUSCLE TRAINERSeptember 26, 1980