Petrarch Systems & Professional Pharm
Country not established
- Devices
- 1
What Petrarch Systems & Professional Pharm makes
Petrarch Systems & Professional Pharm manufactures the OXY-PMMA, a medical device designed for ocular applications, specifically intended for use in corneal transplantation procedures.
The OXY-PMMA is classified as a Class II (U) device under FDA regulations and is listed in the FDA’s 510(k) registry. The company is based in the United States.
Catalogue
Oxy-Pmma Ref K821866
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Petrarch Systems & Professional Pharm have in the registry?
The registry currently lists 1 device for Petrarch Systems & Professional Pharm. Devices recorded under merged duplicate company entries are counted once.
Which registries list Petrarch Systems & Professional Pharm's devices?
Among its 1 most recently registered device, Petrarch Systems & Professional Pharm has devices listed in FDA 510(k) (1 device).
What are the newest devices from Petrarch Systems & Professional Pharm in the registry?
The most recently registered devices listed for Petrarch Systems & Professional Pharm include OXY-PMMA.