The Timeter Group
Country not established
- Devices
- 4
What The Timeter Group makes
The Timeter Group manufactures medical devices for respiratory therapy and fluid administration, including electronic nebulizers, oxygen flowmeters, drip watchers for IV infusion monitoring, and oxygen regulators for hospital and home use.
Their portfolio includes Class I and Class II devices, all of which are subject to FDA 510(k) clearance requirements. The company is based in the United States.
Catalogue
Khm 2000 Drip Watcher Ref K844556
Regimes: 510(k) Registry: 510(k)Classic (Tm) 200 Oxygen Flowmeter Ref K871452
Regimes: 510(k) Registry: 510(k)Mp-500 Electronic Nebulizer Ref K862171
Regimes: 510(k) Registry: 510(k)Oxygen Regulators #50 Prt & Bgt(BGT15, BGT18 Ref K852374
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does The Timeter Group have in the registry?
The registry currently lists 4 devices for The Timeter Group. Devices recorded under merged duplicate company entries are counted once.
Which registries list The Timeter Group's devices?
Among its 4 most recently registered devices, The Timeter Group has devices listed in FDA 510(k) (4 devices).
What risk classes do The Timeter Group's devices fall under?
Among its 4 most recently registered devices, the classes recorded for The Timeter Group's devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from The Timeter Group in the registry?
The most recently registered devices listed for The Timeter Group include KHM 2000 DRIP WATCHER, CLASSIC (TM) 200 OXYGEN FLOWMETER, MP-500 ELECTRONIC NEBULIZER and OXYGEN REGULATORS #50 PRT & BGT(BGT15, BGT18.