DeviceClearance

Product code MZT— Anesthesiology

QUICKAIR CHOKE RELIEVER, MODEL 59-001A

Classification name
Device, Heimlich Maneuver Assist
Device class
Class 2
Regulation
21 CFR 868.5115
Advisory panel
Anesthesiology
Total cleared
1
First cleared
Most recent

Market context for product code MZT

FDA has cleared 1 device under product code MZT, all in 2000, filed by 1 applicant company. No FDA device recalls reference this product code. Class II devices are moderate-risk and subject to general and special controls; most reach market through 510(k) clearance by demonstrating substantial equivalence to a predicate device.

Top applicants under product code MZT

Recent clearances under product code MZT

Data sourced from openFDA. This site is unofficial and independent of the FDA.