510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K900557Substantially Equivalent

Modified Aerochamber M.v. Aerosol Holding Chamber

Monaghan Medical Corp., Plattsburgh NY / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K900557 is the FDA 510(k) clearance record for MODIFIED AEROCHAMBER M.V. AEROSOL HOLDING CHAMBER, a class I device, cleared for Monaghan Medical Corp. on under FDA product code CCQ (Nebulizer, Medicinal, Non-Ventilatory (Atomizer)). FDA records list 35 510(k) clearances for Monaghan Medical Corp., from to . As of , FDA records show no recalls naming K900557.

Clearance record

Decision date
Received
(427 days to decision)
Product code
CCQ Nebulizer, Medicinal, Non-Ventilatory (Atomizer)
Regulation
21 CFR 868.5640
Device class
Class I
Review panel
Anesthesiology
Applicant
Monaghan Medical Corp. Franklyn Bldg., Plattsburgh NY
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