Eyetech M.V.A.
GermanyFDA 510(k) applicant, unverified
- Devices
- 1
What Eyetech M.V.A. makes
Eyetech M.V.A. manufactures the Barraquer-Krumreich Refractive Set, a surgical instrument used in cataract and refractive surgeries for precise corneal incisions and lens extraction procedures.
The Barraquer-Krumreich Refractive Set is classified as a Class I medical device under FDA regulations and is listed in the FDA’s 510(k) clearance database. The company is based in the United States.
Catalogue
Barraquer-Krumeich Refractive Set Ref K954058
510(k) 510(k)
Frequently asked questions
How many devices does Eyetech M.V.A. have in the registry?
The registry currently lists 1 device for Eyetech M.V.A.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Eyetech M.V.A.'s devices?
Among its 1 most recently registered device, Eyetech M.V.A. has devices listed in FDA 510(k) (1 device).
What risk classes do Eyetech M.V.A.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Eyetech M.V.A.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Eyetech M.V.A. in the registry?
The most recently registered devices listed for Eyetech M.V.A. include BARRAQUER-KRUMEICH REFRACTIVE SET.