Windy Hill Technology, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Windy Hill Technology, Inc. makes
Windy Hill Technology, Inc. manufactures the FUJI CATHETER, MODEL CTH001 and the DUCPREP BREAST ASPIRATOR, MODEL PMPO2.
These devices are Class II and listed in the FDA 510(k) registry. Windy Hill Technology, Inc. is based in the US.
Catalogue
Fuji Catheter, Model CTH001 Ref K983867
Regimes: 510(k) Registry: 510(k)Ducprep Breast Aspirator, Model PMPO2 Ref K993342
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Windy Hill Technology, Inc. have in the registry?
The registry currently lists 2 devices for Windy Hill Technology, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Windy Hill Technology, Inc.'s devices?
Among its 2 most recently registered devices, Windy Hill Technology, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Windy Hill Technology, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Windy Hill Technology, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Windy Hill Technology, Inc. in the registry?
The most recently registered devices listed for Windy Hill Technology, Inc. include FUJI CATHETER, MODEL CTH001 and DUCPREP BREAST ASPIRATOR, MODEL PMPO2.