The Phantom Laboratory, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What The Phantom Laboratory, Inc. makes
The Phantom Laboratory, Inc. makes reference phantoms for imaging and radiation therapy, including marks reference phantoms, measure reference phantoms, and radiosurgery verification phantoms.
These devices are classified as Class II medical devices and are listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Radiosurgery Verification Phantom Ref K954634
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does The Phantom Laboratory, Inc. have in the registry?
The registry currently lists 2 devices for The Phantom Laboratory, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list The Phantom Laboratory, Inc.'s devices?
Among its 2 most recently registered devices, The Phantom Laboratory, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do The Phantom Laboratory, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for The Phantom Laboratory, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from The Phantom Laboratory, Inc. in the registry?
The most recently registered devices listed for The Phantom Laboratory, Inc. include MARKS REFERENCE PHANTOM, MEASURE REFERENCE PHANTOM and RADIOSURGERY VERIFICATION PHANTOM.