510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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DEN000004Unknown

Quickair Choke Reliever, Model 59-001A

Maet Industries, Inc., Mississauga, Ontario, CA / Post-NSE, Unknown
FDA source (opens on fda.gov)

DEN000004 is the FDA 510(k) clearance record for QUICKAIR CHOKE RELIEVER, MODEL 59-001A, a class II device, cleared for Maet Industries, Inc. on under FDA product code MZT (Device, Heimlich Maneuver Assist). FDA records list one 510(k) clearance for Maet Industries, Inc. As of , FDA records show no recalls naming DEN000004.

Clearance record

Decision date
Received
(32 days to decision)
Product code
MZT Device, Heimlich Maneuver Assist
Regulation
21 CFR 868.5115
Device class
Class II
Review panel
Anesthesiology
Applicant
Maet Industries, Inc. 4215 Renoak Ct., Mississauga, Ontario, CA
Third party review
No

Clearances, product code MZT

Trailing 12 months

FDA records hold no clearances under product code MZT in the trailing twelve months.

FDA records show no clearances under product code MZT in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code MZT, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260