Incirt Tech., Inc.
Country not established
- Devices
- 1
What Incirt Tech., Inc. makes
Incirt Tech., Inc. manufactures the DLASE 300 UPGRADE, 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
Dlase 300 Upgrade Ref K932065
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Incirt Tech., Inc. have in the registry?
The registry currently lists 1 device for Incirt Tech., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Incirt Tech., Inc.'s devices?
Among its 1 most recently registered device, Incirt Tech., Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Incirt Tech., Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Incirt Tech., Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Incirt Tech., Inc. in the registry?
The most recently registered devices listed for Incirt Tech., Inc. include DLASE 300 UPGRADE.