Linton Biomed Corp.
United StatesFDA applicant, unverified
- Devices
- 5
What Linton Biomed Corp. makes
Linton Biomed Corp. manufactures fluid administration sets, continuous flush devices, and disposable monitoring systems. Their product line also includes injection caps and male luer heparin caps.
These Class II medical devices are listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
Fluid Administrative Set, Afi Ref K820203
Regimes: 510(k) Registry: 510(k)Continuous Flush Device/Fdi Ref K820202
Regimes: 510(k) Registry: 510(k)Dispos. Monitoring Sys/Li Et Al Ref K820201
Regimes: 510(k) Registry: 510(k)Fluid Admin. Set Afs-1C Ref K831348
Regimes: 510(k) Registry: 510(k)Heparin Cap, Injection Cap Male Luer- Ref K841772
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Linton Biomed Corp. have in the registry?
The registry currently lists 5 devices for Linton Biomed Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Linton Biomed Corp.'s devices?
Among its 5 most recently registered devices, Linton Biomed Corp. has devices listed in FDA 510(k) (5 devices).
What risk classes do Linton Biomed Corp.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for Linton Biomed Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Linton Biomed Corp. in the registry?
The most recently registered devices listed for Linton Biomed Corp. include FLUID ADMINISTRATIVE SET, AFI, CONTINUOUS FLUSH DEVICE/FDI, DISPOS. MONITORING SYS/LI ET AL and FLUID ADMIN. SET AFS-1C.