Stewart-Naumann Laboratories
Country not established
- Devices
- 3
What Stewart-Naumann Laboratories makes
Stewart-Naumann Laboratories manufactures disposable syringes in both all-plastic and glass-and-plastic configurations, as well as intravenous infusion pumps designed for controlled fluid administration.
The company’s products are classified as Class II medical devices under FDA regulations, with records supported by 510(k) clearances. The manufacturer is based in the United States.
Catalogue
Syringe, Disposable, All Plastic Ref K760004
Regimes: 510(k) Registry: 510(k)Intravenous Infusion Pump Ref K771300
Regimes: 510(k) Registry: 510(k)Syringe, Disposable, Glass & Plastic Ref K760005
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Stewart-Naumann Laboratories have in the registry?
The registry currently lists 3 devices for Stewart-Naumann Laboratories. Devices recorded under merged duplicate company entries are counted once.
Which registries list Stewart-Naumann Laboratories's devices?
Among its 3 most recently registered devices, Stewart-Naumann Laboratories has devices listed in FDA 510(k) (3 devices).
What risk classes do Stewart-Naumann Laboratories's devices fall under?
Among its 3 most recently registered devices, the classes recorded for Stewart-Naumann Laboratories's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Stewart-Naumann Laboratories in the registry?
The most recently registered devices listed for Stewart-Naumann Laboratories include SYRINGE, DISPOSABLE, ALL PLASTIC, INTRAVENOUS INFUSION PUMP and SYRINGE, DISPOSABLE, GLASS & PLASTIC.