Diagnostic Instrument Corp.
United StatesFDA applicant, unverified
- Devices
- 2
What Diagnostic Instrument Corp. makes
Diagnostic Instrument Corp. produces medical imaging coils, including the DIAGNOSTIC INSTRUMENTS INC. MODEL T803 BREAST COIL and the MODEL GP-252 GENERAL PURPOSE COIL.
These devices are Class II and listed in the FDA 510(k) registry. The company is based in the US.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Model Gp-252 General Purpose Coil Ref K935691
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Diagnostic Instrument Corp. have in the registry?
The registry currently lists 2 devices for Diagnostic Instrument Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Diagnostic Instrument Corp.'s devices?
Among its 2 most recently registered devices, Diagnostic Instrument Corp. has devices listed in FDA 510(k) (2 devices).
What risk classes do Diagnostic Instrument Corp.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Diagnostic Instrument Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Diagnostic Instrument Corp. in the registry?
The most recently registered devices listed for Diagnostic Instrument Corp. include DIAGNOSTIC INSTRUMLENTS INC. MODEL T803 BREAST COIL and MODEL GP-252 GENERAL PURPOSE COIL.