Lazarus Effect, Inc.
Country not established
- Devices
- 1
What Lazarus Effect, Inc. makes
Lazarus Effect, Inc. produces the FUNNEL GUIDE CATHETER MODEL G1020608, which is a Class II medical device.
The company is based in the US and its device is listed in the FDA 510(k) registry.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Funnel Guide Catheter Model G1020608 Ref K102439
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Lazarus Effect, Inc. have in the registry?
The registry currently lists 1 device for Lazarus Effect, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Lazarus Effect, Inc.'s devices?
Among its 1 most recently registered device, Lazarus Effect, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Lazarus Effect, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Lazarus Effect, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Lazarus Effect, Inc. in the registry?
The most recently registered devices listed for Lazarus Effect, Inc. include FUNNEL GUIDE CATHETER MODEL G1020608.