Pathwai, Inc.
United Statesfrom the FDA registration address FDA FEI 3046433998
- Devices
- 2
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Registry: GUDID
EchoNext Ref K260332
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3046433998
- DUNS number
- 145078546
- Address
- 189 W 89th Street, New York, NY, 10024
Frequently asked questions
How many devices does Pathwai, Inc. have in the registry?
The registry currently lists 2 devices for Pathwai, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Pathwai, Inc.'s devices?
Among its 2 most recently registered devices, Pathwai, Inc. has devices listed in FDA 510(k) (1 device) and FDA GUDID (1 device). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Pathwai, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Pathwai, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Pathwai, Inc. in the registry?
The most recently registered devices listed for Pathwai, Inc. include EchoNext 00 and EchoNext.