Intersep, Ltd.
United KingdomFDA applicant, unverified
- Devices
- 1
What Intersep, Ltd. makes
Intersep, Ltd. manufactures the NANOSEP N10, a filtration device designed for sterile filtration of liquids, including pharmaceutical and biotechnology applications.
The NANOSEP N10 is classified as a Class I 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
Nanosep N10 Ref K935496
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Intersep, Ltd. have in the registry?
The registry currently lists 1 device for Intersep, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Intersep, Ltd.'s devices?
Among its 1 most recently registered device, Intersep, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Intersep, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Intersep, Ltd.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Intersep, Ltd. in the registry?
The most recently registered devices listed for Intersep, Ltd. include NANOSEP N10.