Interneuron Pharmaceuticals, Inc.
Country not established
- Devices
- 1
What Interneuron Pharmaceuticals, Inc. makes
Interneuron Pharmaceuticals, Inc. manufactures the Anatomark Noninvasive Head Reference System, a device designed to provide precise anatomical localization for medical imaging and procedural guidance in neurosurgical applications.
The Anatomark system is classified as a Class II medical device under FDA regulations and is supported by a 510(k) clearance. The company is based in the United States.
Catalogue
Anatomark Noninvasive Head Reference System Ref K981398
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Interneuron Pharmaceuticals, Inc. have in the registry?
The registry currently lists 1 device for Interneuron Pharmaceuticals, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Interneuron Pharmaceuticals, Inc.'s devices?
Among its 1 most recently registered device, Interneuron Pharmaceuticals, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Interneuron Pharmaceuticals, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Interneuron Pharmaceuticals, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Interneuron Pharmaceuticals, Inc. in the registry?
The most recently registered devices listed for Interneuron Pharmaceuticals, Inc. include ANATOMARK NONINVASIVE HEAD REFERENCE SYSTEM.