Midwest Ophthalmic Instruments, Inc.
Country not established
- Devices
- 1
What Midwest Ophthalmic Instruments, Inc. makes
Midwest Ophthalmic Instruments, Inc. manufactures the ORIMS DIGITAL ANGIOGRAPHY SYSTEM, which is a medical device used for digital angiography procedures.
The company's products are regulated as Class II devices and are listed in the FDA 510(k) registry. Midwest Ophthalmic Instruments, Inc. is based in the US.
Catalogue
Orims Digital Angiography System Ref K952480
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Midwest Ophthalmic Instruments, Inc. have in the registry?
The registry currently lists 1 device for Midwest Ophthalmic Instruments, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Midwest Ophthalmic Instruments, Inc.'s devices?
Among its 1 most recently registered device, Midwest Ophthalmic Instruments, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Midwest Ophthalmic Instruments, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Midwest Ophthalmic Instruments, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Midwest Ophthalmic Instruments, Inc. in the registry?
The most recently registered devices listed for Midwest Ophthalmic Instruments, Inc. include ORIMS DIGITAL ANGIOGRAPHY SYSTEM.