Smiths Medical Ads, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
Catalogue
- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Smiths Medical Ads, Inc. have in the registry?
The registry currently lists 2 devices for Smiths Medical Ads, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Smiths Medical Ads, Inc.'s devices?
Among its 2 most recently registered devices, Smiths Medical Ads, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Smiths Medical Ads, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Smiths Medical Ads, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Smiths Medical Ads, Inc. in the registry?
The most recently registered devices listed for Smiths Medical Ads, Inc. include BLUselect, non-fenestrated, BLUselect, non-fenestrated, cont, BLUselect, fenestrated, BLUselect Suctionaid, BLUpere Dilation Trachestomy Kit, without tube and CADD®- Solis Ambulatory Infusion Pump with Wireless Communication; CADD®-Solis Infusion Pump, Model 2110; PharmGuard® Administrator Medication Safety Software; CADD® Administration Sets; Wireless Communication Module (CM).