Barron Precision Instruments, LLC
Country not established
- Devices
- 1
What Barron Precision Instruments, LLC makes
Barron Precision Instruments, LLC manufactures the BARRON MICROKERATOME SYSTEM, Model B2000, a surgical device used for precise corneal cutting in ophthalmic procedures.
The BARRON MICROKERATOME SYSTEM, Model B2000 is classified as a Class I medical device in the US and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Barron Microkeratome System, Model B2000 Ref K983317
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Barron Precision Instruments, LLC have in the registry?
The registry currently lists 1 device for Barron Precision Instruments, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Barron Precision Instruments, LLC's devices?
Among its 1 most recently registered device, Barron Precision Instruments, LLC has devices listed in FDA 510(k) (1 device).
What risk classes do Barron Precision Instruments, LLC's devices fall under?
Among its 1 most recently registered device, the classes recorded for Barron Precision Instruments, LLC's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Barron Precision Instruments, LLC in the registry?
The most recently registered devices listed for Barron Precision Instruments, LLC include BARRON MICROKERATOME SYSTEM, MODEL B2000.