MZT — Device, Heimlich Maneuver Assist Class II

FDA Device Classification

FDA product code MZT covers "Device, Heimlich Maneuver Assist", a Class II medical device regulated under 21 CFR 868.5115. Submissions are reviewed by the Anesthesiology panel. At least 1 recent 510(k) clearance has been granted under this product code.

Classification Details

Product Code
MZT
Device Class
Class II
Regulation Number
868.5115
Submission Type
Review Panel
AN
Medical Specialty
Anesthesiology
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
DEN000004maet industriesQUICKAIR CHOKE RELIEVER, MODEL 59-001AFebruary 29, 2000