Howard K. Mann & Assoc.
Country not established
- Devices
- 1
What Howard K. Mann & Assoc. makes
Howard K. Mann & Assoc. manufactures the MASTER-NEB Nebulizer Compressor System, a Class II medical device designed for aerosolizing liquid medications into fine particles for inhalation therapy.
The device is regulated under FDA 510(k) clearance as a Class II product and is listed in the U.S. regulatory database. The company is based in the United States.
Catalogue
Master-Neb Nebulizer Compressor System Ref K943717
510(k) 510(k)
Frequently asked questions
How many devices does Howard K. Mann & Assoc. have in the registry?
The registry currently lists 1 device for Howard K. Mann & Assoc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Howard K. Mann & Assoc.'s devices?
Among its 1 most recently registered device, Howard K. Mann & Assoc. has devices listed in FDA 510(k) (1 device).
What risk classes do Howard K. Mann & Assoc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Howard K. Mann & Assoc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Howard K. Mann & Assoc. in the registry?
The most recently registered devices listed for Howard K. Mann & Assoc. include MASTER-NEB NEBULIZER COMPRESSOR SYSTEM.