Pressure Products, Inc.
United Statesfrom the FDA registration address FDA establishment FEI 2025881
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 2025881
- Address
- 49 Via Alicia, Santa Barbara, CA, 93108
Frequently asked questions
How many devices does PRESSURE PRODUCTS, INC. have in the registry?
The registry currently lists 1 device for PRESSURE PRODUCTS, INC.. Devices recorded under merged duplicate company entries are counted once.
Which registries list PRESSURE PRODUCTS, INC.'s devices?
Among its 1 most recently registered device, PRESSURE PRODUCTS, INC. has devices listed in FDA 510(k) (1 device).
What risk classes do PRESSURE PRODUCTS, INC.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for PRESSURE PRODUCTS, INC.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from PRESSURE PRODUCTS, INC. in the registry?
The most recently registered devices listed for PRESSURE PRODUCTS, INC. include PRESDURE PRODUCTS PRESSURE PADS, MODELS P100, P110, P120, P130, P200, P210, P220, P230, P300, P310, P320, P330.