Path Scientific
Country not established FDA establishment FEI 3006760998
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
What Path Scientific makes
PATH Scientific manufactures the PATHFORMER, a medical device designed for use in surgical procedures, likely as a tissue or organ support system during transplantation or reconstructive surgery.
The PATHFORMER is classified as a Class I device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
Pathformer Ref K052770
510(k) 510(k)
Company details
- FDA FEI number
- 3006760998
- Address
- Path Scientific, Carlisle, MA, 01741
Frequently asked questions
How many devices does PATH SCIENTIFIC have in the registry?
The registry currently lists 1 device for PATH SCIENTIFIC. Devices recorded under merged duplicate company entries are counted once.
Which registries list PATH SCIENTIFIC's devices?
Among its 1 most recently registered device, PATH SCIENTIFIC has devices listed in FDA 510(k) (1 device).
What risk classes do PATH SCIENTIFIC's devices fall under?
Among its 1 most recently registered device, the classes recorded for PATH SCIENTIFIC's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from PATH SCIENTIFIC in the registry?
The most recently registered devices listed for PATH SCIENTIFIC include PATHFORMER.