Eg&G Ortec, Inc.
Country not established
- Devices
- 1
What Eg&G Ortec, Inc. makes
Eg&G Ortec, Inc. manufactures the NEURO-ECAT, a device designed for nuclear medicine imaging, likely used in positron emission tomography (PET) or similar diagnostic applications.
The NEURO-ECAT is classified as a Class II medical device under FDA regulations and is listed in the 510(k) clearance database. The company is based in the United States.
Catalogue
Neuro-Ecat Ref K810589
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Eg&G Ortec, Inc. have in the registry?
The registry currently lists 1 device for Eg&G Ortec, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Eg&G Ortec, Inc.'s devices?
Among its 1 most recently registered device, Eg&G Ortec, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Eg&G Ortec, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Eg&G Ortec, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Eg&G Ortec, Inc. in the registry?
The most recently registered devices listed for Eg&G Ortec, Inc. include NEURO-ECAT.