Par Medizintechnik GmbH
GermanyFDA applicant, unverified
- Devices
- 1
What Par Medizintechnik GmbH makes
Par Medizintechnik GmbH manufactures the TONOPORT V, a device designed for measuring intraocular pressure in ophthalmology, aiding in the diagnosis and monitoring of glaucoma.
The TONOPORT V is classified as a Class II medical device and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Tonoport V Ref K012647
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Par Medizintechnik GmbH have in the registry?
The registry currently lists 1 device for Par Medizintechnik GmbH. Devices recorded under merged duplicate company entries are counted once.
Which registries list Par Medizintechnik GmbH's devices?
Among its 1 most recently registered device, Par Medizintechnik GmbH has devices listed in FDA 510(k) (1 device).
What risk classes do Par Medizintechnik GmbH's devices fall under?
Among its 1 most recently registered device, the classes recorded for Par Medizintechnik GmbH's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Par Medizintechnik GmbH in the registry?
The most recently registered devices listed for Par Medizintechnik GmbH include TONOPORT V.