Konica Medical and Graphic Corporation
JapanFDA applicant, unverified
- Devices
- 1
What Konica Medical and Graphic Corporation makes
Konica Medical and Graphic Corporation manufactures the Konica Laser Imager, specifically the DRYPRO Model 771, a device designed for medical imaging applications.
The company’s portfolio is regulated under FDA’s Class II device classification, with the DRYPRO Model 771 listed via a 510(k) submission. The manufacturer operates from the United States.
Catalogue
Konica Laser Imager, Model Drypro Model 771 Ref K032681
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Konica Medical and Graphic Corporation have in the registry?
The registry currently lists 1 device for Konica Medical and Graphic Corporation. Devices recorded under merged duplicate company entries are counted once.
Which registries list Konica Medical and Graphic Corporation's devices?
Among its 1 most recently registered device, Konica Medical and Graphic Corporation has devices listed in FDA 510(k) (1 device).
What risk classes do Konica Medical and Graphic Corporation's devices fall under?
Among its 1 most recently registered device, the classes recorded for Konica Medical and Graphic Corporation's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Konica Medical and Graphic Corporation in the registry?
The most recently registered devices listed for Konica Medical and Graphic Corporation include KONICA LASER IMAGER, MODEL DRYPRO MODEL 771.