Q-Core, Ltd.
IsraelFDA 510(k) applicant, unverified
- Devices
- 1
What Q-Core, Ltd. makes
Q-Core, Ltd. manufactures the AP 34 Multi-Therapy Infusion Pump, a device designed for delivering multiple therapies via controlled infusion in clinical settings.
The AP 34 Multi-Therapy Infusion Pump is classified as a Class II device under FDA regulations and is listed in the 510(k) clearance registry. The company is based in the United States.
Catalogue
Ap 34 Multi-Therapy Infusion Pump Ref K082182
510(k) 510(k)
Frequently asked questions
How many devices does Q-Core, Ltd. have in the registry?
The registry currently lists 1 device for Q-Core, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Q-Core, Ltd.'s devices?
Among its 1 most recently registered device, Q-Core, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Q-Core, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Q-Core, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Q-Core, Ltd. in the registry?
The most recently registered devices listed for Q-Core, Ltd. include AP 34 MULTI-THERAPY INFUSION PUMP.