Delta Medical Manuf, Inc.
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- Devices
- 1
What Delta Medical Manuf, Inc. makes
Delta Medical Manuf, Inc. produces the 3P Pulmonary Percussive Pack, a device designed for percussive therapy to assist with airway clearance in patients with respiratory conditions.
The company’s portfolio is regulated under FDA Class II devices and includes products listed via the 510(k) clearance pathway. Delta Medical Manuf, Inc. is based in the United States.
Catalogue
3P (Pulmonary Percussive Pack) Ref K931988
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Delta Medical Manuf, Inc. have in the registry?
The registry currently lists 1 device for Delta Medical Manuf, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Delta Medical Manuf, Inc.'s devices?
Among its 1 most recently registered device, Delta Medical Manuf, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Delta Medical Manuf, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Delta Medical Manuf, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Delta Medical Manuf, Inc. in the registry?
The most recently registered devices listed for Delta Medical Manuf, Inc. include 3P (PULMONARY PERCUSSIVE PACK).