General Scanning, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What General Scanning, Inc. makes
General Scanning, Inc. manufactures nuclear medicine imaging devices, including laser-based imagers for diagnostic use. Their product line includes the DIGMI-2000 (internal reference LD2800) and the LD2000 series, designed for medical imaging applications.
These devices are classified as Class II under US regulations and are listed via FDA 510(k) clearance. The company operates from the United States.
Catalogue
Nuclear Medicine Laser Imager Ref K923536
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
LD2000 Series Ref K980565
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does General Scanning, Inc. have in the registry?
The registry currently lists 3 devices for General Scanning, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list General Scanning, Inc.'s devices?
Among its 3 most recently registered devices, General Scanning, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do General Scanning, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for General Scanning, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from General Scanning, Inc. in the registry?
The most recently registered devices listed for General Scanning, Inc. include NUCLEAR MEDICINE LASER IMAGER, DIGMI-2000 (GSI INTERNAL REFERENCE)/LD2800 (MARKETING NAME) and LD2000 SERIES.