← Back to catalogue

Modified Aerochamber M.v. Aerosol Holding Chamber

FDA 510(k)

Class I (US FDA 510(k))

510(k) K900557

by Monaghan Medical Corp.

Identifiers

510(k) Number
K900557 FDA 510(k)
FDA Product Code
CCQ FDA 510(k)

Classification

Device Class
Class I FDA 510(k)
Legislation / Framework
21 CFR Part 868.5640 FDA 510(k)
Regulation Number
868.5640 FDA 510(k)
Advisory Committee
Anesthesiology FDA 510(k)
FDA Decision
SESE Substantially Equivalent FDA 510(k)

Modified Aerochamber M.v. Aerosol Holding Chamber by Monaghan Medical Corp. — Class I — FDA_510K — listed in FDA 510(k) — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Active

FDA_510K

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA 510(k) K900557 24 fields · synced Jun 18, 2026