Peermedical, Ltd.
IsraelFDA applicant, unverified
- Devices
- 2
What Peermedical, Ltd. makes
Peermedical, Ltd. manufactures the PEERSCOPE SYSTEM, a medical device designed for endoscopic visualization and procedural guidance in clinical settings.
The PEERSCOPE SYSTEM is classified as a Class II device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
Peerscope System Ref K120289
Regimes: 510(k) Registry: 510(k)Peerscope System Ref K130718
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Peermedical, Ltd. have in the registry?
The registry currently lists 2 devices for Peermedical, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Peermedical, Ltd.'s devices?
Among its 2 most recently registered devices, Peermedical, Ltd. has devices listed in FDA 510(k) (2 devices).
What risk classes do Peermedical, Ltd.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Peermedical, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Peermedical, Ltd. in the registry?
The most recently registered devices listed for Peermedical, Ltd. include PEERSCOPE SYSTEM.