Medivice Systems, Ltd.
IsraelFDA applicant, unverified
- Devices
- 1
What Medivice Systems, Ltd. makes
Medivice Systems, Ltd. manufactures the Sideport Pinch Clamp Device, a medical instrument designed for securing and isolating vascular access ports during procedures.
The Sideport Pinch Clamp Device is classified as a Class II medical device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
Sideport Pinch Clamp Device Ref K010888
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Medivice Systems, Ltd. have in the registry?
The registry currently lists 1 device for Medivice Systems, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medivice Systems, Ltd.'s devices?
Among its 1 most recently registered device, Medivice Systems, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Medivice Systems, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Medivice Systems, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Medivice Systems, Ltd. in the registry?
The most recently registered devices listed for Medivice Systems, Ltd. include SIDEPORT PINCH CLAMP DEVICE.