Turboseal, L.P.
IsraelFDA 510(k) applicant, unverified
- Devices
- 1
What Turboseal, L.P. makes
Turboseal, L.P. manufactures the TurboSEAL Nasogastric Aspiration Tube, a device designed for gastric drainage and aspiration in clinical settings. It incorporates a specialized seal mechanism to reduce leakage and contamination risks during use.
The TurboSEAL Nasogastric Aspiration Tube is classified as a Class II medical device under FDA regulations and is listed via a 510(k) clearance. The company is based in the United States.
Catalogue
TurboSEAL Nasogastric Aspiration Tube Ref K142483
510(k) 510(k)
Frequently asked questions
How many devices does Turboseal, L.P. have in the registry?
The registry currently lists 1 device for Turboseal, L.P.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Turboseal, L.P.'s devices?
Among its 1 most recently registered device, Turboseal, L.P. has devices listed in FDA 510(k) (1 device).
What risk classes do Turboseal, L.P.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Turboseal, L.P.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Turboseal, L.P. in the registry?
The most recently registered devices listed for Turboseal, L.P. include TurboSEAL Nasogastric Aspiration Tube.