Q-Life Systems, Inc.
CanadaFDA 510(k) applicant, unverified
- Devices
- 2
What Q-Life Systems, Inc. makes
Q-Life Systems, Inc. manufactures the PARTNER Infusion System, a volumetric infusion pump designed for epidural drug delivery. The device is intended for controlled administration of medications through epidural catheters, supporting continuous or intermittent infusion protocols in clinical settings.
The PARTNER Infusion System is classified as a Class II medical device in the U.S. and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Partner Infusion System: Ref K896717
510(k) 510(k)- 510(k) 510(k)
Frequently asked questions
How many devices does Q-Life Systems, Inc. have in the registry?
The registry currently lists 2 devices for Q-Life Systems, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Q-Life Systems, Inc.'s devices?
Among its 2 most recently registered devices, Q-Life Systems, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Q-Life Systems, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Q-Life Systems, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Q-Life Systems, Inc. in the registry?
The most recently registered devices listed for Q-Life Systems, Inc. include PARTNER INFUSION SYSTEM: and EPIDURAL INDICATION FOR VOLUMETRIC INFUSION PUMPS.