Micro Direct, Inc.
United StatesFDA applicant, unverified FDA FEI 1000305581
- Devices
- 9
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Micro Mpm Ref K940375
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Micro H2 Ref K963376
Regimes: 510(k) Registry: 510(k)Microlab Spirometer Ref K031102
Regimes: 510(k) Registry: 510(k)Spirosafe Filter Ref K973314
Regimes: 510(k) Registry: 510(k)Micropeak Ref K030586
Regimes: 510(k) Registry: 510(k)Microco Ref K950197
Regimes: 510(k) Registry: 510(k)Micro Spirometer Ref K963035
Regimes: 510(k) Registry: 510(k)Microdl Diarycard Spirometer Ref K965042
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 1000305581
- Address
- 803 WEBSTER ST, LEWISTON, ME, 04240
Frequently asked questions
How many devices does Micro Direct, Inc. have in the registry?
The registry currently lists 9 devices for Micro Direct, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Micro Direct, Inc.'s devices?
Among its 9 most recently registered devices, Micro Direct, Inc. has devices listed in FDA 510(k) (9 devices).
What risk classes do Micro Direct, Inc.'s devices fall under?
Among its 9 most recently registered devices, the classes recorded for Micro Direct, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Micro Direct, Inc. in the registry?
The most recently registered devices listed for Micro Direct, Inc. include MICRO MPM, MICRO H2 BREATH MONITORING DEVICE WITH HYDRA SOFTWARE UTILITY, MICRO H2 and MICROLAB SPIROMETER.