Design Technologies, Inc.
United StatesFDA applicant, unverified
- Devices
- 4
What Design Technologies, Inc. makes
Design Technologies, Inc. manufactures respiratory therapy devices, including the NO-FLO I and MODIFIED NOFLO I for aerosolized medication delivery, the NEB-U-VENT for nebulizer ventilation, and the STA-PUT for securing medical tubing.
These devices are classified as Class I under FDA regulations and are listed via 510(k) clearance. The company is based in the United States.
Catalogue
No-Flo I Ref K863613
Regimes: 510(k) Registry: 510(k)Modified Noflo I Ref K871262
Regimes: 510(k) Registry: 510(k)Neb-U-Vent Ref K872038
Regimes: 510(k) Registry: 510(k)Sta-Put Ref K872358
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Design Technologies, Inc. have in the registry?
The registry currently lists 4 devices for Design Technologies, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Design Technologies, Inc.'s devices?
Among its 4 most recently registered devices, Design Technologies, Inc. has devices listed in FDA 510(k) (4 devices).
What risk classes do Design Technologies, Inc.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Design Technologies, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Design Technologies, Inc. in the registry?
The most recently registered devices listed for Design Technologies, Inc. include NO-FLO I, MODIFIED NOFLO I, NEB-U-VENT and STA-PUT.