Shotwell & Carr, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What Shotwell & Carr, Inc. makes
Shotwell & Carr, Inc. manufactures diagnostic imaging and analysis devices, including the SMART WAVE GS100 for ultrasound-based imaging, the MDX 2000 Digital Analyzer for medical signal processing, and the DTX-200 Bone Densitometer for bone density measurements.
These devices are classified as Class II under FDA regulations and are supported by 510(k) clearance records. The company operates within the United States.
Catalogue
Smart Wave GS100 Ref K950617
Regimes: 510(k) Registry: 510(k)Mdx 2000, Digital Analyzer Ref K970824
Regimes: 510(k) Registry: 510(k)Dtx-200 Bone Densitometer Ref K961011
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Shotwell & Carr, Inc. have in the registry?
The registry currently lists 3 devices for Shotwell & Carr, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Shotwell & Carr, Inc.'s devices?
Among its 3 most recently registered devices, Shotwell & Carr, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Shotwell & Carr, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Shotwell & Carr, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Shotwell & Carr, Inc. in the registry?
The most recently registered devices listed for Shotwell & Carr, Inc. include SMART WAVE GS100, MDX 2000, DIGITAL ANALYZER and DTX-200 BONE DENSITOMETER.