S & S X-Ray Products, Inc.
United StatesFDA applicant, unverified
- Devices
- 4
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Squeeze-Ease Mammography Cushion Ref K031574
Regimes: 510(k) Registry: 510(k)Planet Thermoplastic Immobilization System Ref K944040
Regimes: 510(k) Registry: 510(k)Sand S MB12 Mammography Moving Grid Bucky Ref K850614
Regimes: 510(k) Registry: 510(k)- Regimes: CE MDR 510(k) Registry: 510(k)
Frequently asked questions
How many devices does S & S X-Ray Products, Inc. have in the registry?
The registry currently lists 4 devices for S & S X-Ray Products, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list S & S X-Ray Products, Inc.'s devices?
Among its 4 most recently registered devices, S & S X-Ray Products, Inc. has devices listed in FDA 510(k) (4 devices).
What risk classes do S & S X-Ray Products, Inc.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for S & S X-Ray Products, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from S & S X-Ray Products, Inc. in the registry?
The most recently registered devices listed for S & S X-Ray Products, Inc. include SQUEEZE-EASE MAMMOGRAPHY CUSHION, PLANET THERMOPLASTIC IMMOBILIZATION SYSTEM, SAND S MB12 MAMMOGRAPHY MOVING GRID BUCKY and DCD-1 (DIGITAL CONTOUR DETECT-RADIAT THERAPY) SYST.