Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K841321Substantially Equivalent

Air-Neb Nebulizer Compressor Unit

Airmed Corp., Mchenry IL / Traditional, Substantially Equivalent

K841321 is the FDA 510(k) clearance record for AIR-NEB NEBULIZER COMPRESSOR UNIT, a class I device, cleared for Airmed Corp. on under FDA product code CCQ (Nebulizer, Medicinal, Non-Ventilatory (Atomizer)). FDA records list 3 510(k) clearances for Airmed Corp., from to . As of , FDA records show no recalls naming K841321.

Clearance record

Decision date
Received
(11 days to decision)
Product code
CCQ Nebulizer, Medicinal, Non-Ventilatory (Atomizer)
Regulation
21 CFR 868.5640
Device class
Class I
Review panel
Anesthesiology
Applicant
Airmed Corp. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code CCQ

Trailing 12 months

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

FDA records show no clearances under product code CCQ in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code CCQ, 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