Diagnostic Devices, Inc.
Country not established
- Devices
- 4
What Diagnostic Devices, Inc. makes
Diagnostic Devices, Inc. manufactures blood glucose monitoring systems, including a handheld test system and a voice-enabled monitoring solution for real-time glucose tracking. The company also produces an ultrasonic nebulizer system for respiratory therapy.
These devices are classified as Class II under FDA regulations and are listed via 510(k) clearance. The company is based in the United States.
Catalogue
Prodigy Blood Glucose Test System Ref K060467
Regimes: 510(k) Registry: 510(k)Prodigy Voice Blood Glucose Monitoring System Ref K073118
Regimes: 510(k) Registry: 510(k)Ddi Ultrasonic Nebulizer System Ref K090307
Regimes: 510(k) Registry: 510(k)Prodigy Ref K053593
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Diagnostic Devices, Inc. have in the registry?
The registry currently lists 4 devices for Diagnostic Devices, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Diagnostic Devices, Inc.'s devices?
Among its 4 most recently registered devices, Diagnostic Devices, Inc. has devices listed in FDA 510(k) (4 devices).
What risk classes do Diagnostic Devices, Inc.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Diagnostic Devices, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Diagnostic Devices, Inc. in the registry?
The most recently registered devices listed for Diagnostic Devices, Inc. include PRODIGY BLOOD GLUCOSE TEST SYSTEM, PRODIGY VOICE BLOOD GLUCOSE MONITORING SYSTEM, DDI ULTRASONIC NEBULIZER SYSTEM and PRODIGY.