Newport Biosystems, Inc.
United StatesFDA applicant, unverified
- Devices
- 5
What Newport Biosystems, Inc. makes
Newport Biosystems, Inc. produces tissue culture media, including RPMI 1640 with glutamine and HEPES, as well as fetal bovine serum in transfer containers. The company also supplies transfer container humidifiers for laboratory use.
These products are regulated as Class I and Class II devices under FDA 510(k) clearance requirements. The company is based in the United States.
Catalogue
Tissue Culture Media Ref K855085
Regimes: 510(k) Registry: 510(k)Rpmi 1640 W/Glutamine W/Hepes Ref K860282
Regimes: 510(k) Registry: 510(k)Transfer Container Humidifier Ref K881648
Regimes: 510(k) Registry: 510(k)Newport Media Transfer Container Ref K852532
Regimes: 510(k) Registry: 510(k)Fetal Bovine Serum In Transfer Container Ref K853441
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Newport Biosystems, Inc. have in the registry?
The registry currently lists 5 devices for Newport Biosystems, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Newport Biosystems, Inc.'s devices?
Among its 5 most recently registered devices, Newport Biosystems, Inc. has devices listed in FDA 510(k) (5 devices).
What risk classes do Newport Biosystems, Inc.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for Newport Biosystems, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Newport Biosystems, Inc. in the registry?
The most recently registered devices listed for Newport Biosystems, Inc. include TISSUE CULTURE MEDIA, RPMI 1640 W/GLUTAMINE W/HEPES, TRANSFER CONTAINER HUMIDIFIER and NEWPORT MEDIA TRANSFER CONTAINER.