Q For Plastic Industries
EgyptFDA 510(k) applicant, unverified
- Devices
- 1
What Q For Plastic Industries makes
Q For Plastic Industries manufactures the ResQ Administration Set, a sterile, single-use intravenous administration device designed for fluid and medication delivery in clinical settings.
The ResQ Administration Set 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
ResQ Administration Set Ref K231707
510(k) 510(k)
Frequently asked questions
How many devices does Q For Plastic Industries have in the registry?
The registry currently lists 1 device for Q For Plastic Industries. Devices recorded under merged duplicate company entries are counted once.
Which registries list Q For Plastic Industries's devices?
Among its 1 most recently registered device, Q For Plastic Industries has devices listed in FDA 510(k) (1 device).
What risk classes do Q For Plastic Industries's devices fall under?
Among its 1 most recently registered device, the classes recorded for Q For Plastic Industries's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Q For Plastic Industries in the registry?
The most recently registered devices listed for Q For Plastic Industries include ResQ Administration Set.