Microsonic, Inc.
United StatesFDA applicant, unverified FDA FEI 2523819
- Devices
- 2
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Microsil Ref K945255
Regimes: 510(k) Registry: 510(k)Mega-Sil A-B Ref K950912
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 2523819
- Address
- 2960 DUSS AVE., AMBRIDGE, PA, 15003
Frequently asked questions
How many devices does Microsonic, Inc. have in the registry?
The registry currently lists 2 devices for Microsonic, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Microsonic, Inc.'s devices?
Among its 2 most recently registered devices, Microsonic, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Microsonic, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Microsonic, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Microsonic, Inc. in the registry?
The most recently registered devices listed for Microsonic, Inc. include MICROSIL and MEGA-SIL A-B.