Glaxo, Inc.
United StatesFDA applicant, unverified
- Devices
- 4
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Volumatic Ref K844169
Regimes: 510(k) Registry: 510(k)Syringe Needle Introducer Ref K901803
Regimes: 510(k) Registry: 510(k)Compact Spacer Ref K922187
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Glaxo, Inc. have in the registry?
The registry currently lists 4 devices for Glaxo, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Glaxo, Inc.'s devices?
Among its 4 most recently registered devices, Glaxo, Inc. has devices listed in FDA 510(k) (4 devices).
What risk classes do Glaxo, Inc.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Glaxo, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Glaxo, Inc. in the registry?
The most recently registered devices listed for Glaxo, Inc. include VOLUMATIC, SYRINGE NEEDLE INTRODUCER, COMPACT SPACER and G.R.E.E.N. DISPOSAL CONTAINER (NOTE: G.R.E.E.N. IS AN ACRONYM FOR GLAXO RETRIEVAL EFFORT FOR EXPENDED NEEDLES).