510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K810939Substantially Equivalent

Nebulizer/humidifier Humidity Center-Mi.

Allied Medical LLC, Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K810939 is the FDA 510(k) clearance record for NEBULIZER/HUMIDIFIER HUMIDITY CENTER-MI., a class II device, cleared for Allied Healthcare Products, Inc. on under FDA product code BTT (Humidifier, Respiratory Gas, (Direct Patient Interface)). FDA records list 26 510(k) clearances for Allied Medical LLC, from to . As of , FDA records show no recalls naming K810939.

Clearance record

Decision date
Received
(16 days to decision)
Product code
BTT Humidifier, Respiratory Gas, (Direct Patient Interface)
Regulation
21 CFR 868.5450
Device class
Class II
Review panel
Anesthesiology
Applicant
Allied Healthcare Products, Inc. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code BTT

Trailing 12 months
5 clearances under product code BTT in the twelve months to October 2026, January 2026 the highest month at 2.
Show the numbers
Monthly 510(k) clearances under FDA product code BTT, trailing twelve months
MonthClearances
November 20250
December 20251
January 20262
February 20260
March 20260
April 20261
May 20260
June 20260
July 20260
August 20261
September 20260
October 20260