Maguire Ent., Inc.
United Statesfrom the FDA registration address FDA FEI 1049754
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Ecg Modulator Ref K922412
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 1049754
- Address
- 10289 NW 46TH STREET, FORT LAUDERDALE, FL, 33351
Frequently asked questions
How many devices does Maguire Ent., Inc. have in the registry?
The registry currently lists 1 device for Maguire Ent., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Maguire Ent., Inc.'s devices?
Among its 1 most recently registered device, Maguire Ent., Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Maguire Ent., Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Maguire Ent., Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Maguire Ent., Inc. in the registry?
The most recently registered devices listed for Maguire Ent., Inc. include ECG MODULATOR.