Precise Medical Products, Ltd.
IsraelFDA applicant, unverified
- Devices
- 2
What Precise Medical Products, Ltd. makes
Precise Medical Products, Ltd. manufactures the SMARTINFUSER PAINPUMP, offered as model P49220 with a catheter set and model P49224N without a catheter set. These are programmable infusion devices designed for pain management.
The devices are classified as Class II medical devices and are listed in the FDA 510(k) registry. The company is based in the United States. This record supports the regulatory listing.
Catalogue
Smartinfuser Painpump Ref K042122
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Precise Medical Products, Ltd. have in the registry?
The registry currently lists 2 devices for Precise Medical Products, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Precise Medical Products, Ltd.'s devices?
Among its 2 most recently registered devices, Precise Medical Products, Ltd. has devices listed in FDA 510(k) (2 devices).
What risk classes do Precise Medical Products, Ltd.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Precise Medical Products, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Precise Medical Products, Ltd. in the registry?
The most recently registered devices listed for Precise Medical Products, Ltd. include SMARTINFUSER PAINPUMP and SMARTINFUSER PAINPUMP, MODEL P49220 W/CATHETER SET; P49224N W/O CATHETER SET.