Polaroid Medical Corp.
Country not established
- Devices
- 1
What Polaroid Medical Corp. makes
Polaroid Medical Corp. manufactures the Polaroid Helios Laser Imager, a device designed for capturing high-resolution images of internal anatomical structures using laser technology, primarily for diagnostic and procedural guidance purposes.
The Helios Laser Imager is classified as a Class II medical device under FDA regulations and is authorised via the 510(k) pathway. The company is based in the United States.
Catalogue
Polaroid Helios Laser Imager Ref K912073
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Polaroid Medical Corp. have in the registry?
The registry currently lists 1 device for Polaroid Medical Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Polaroid Medical Corp.'s devices?
Among its 1 most recently registered device, Polaroid Medical Corp. has devices listed in FDA 510(k) (1 device).
What risk classes do Polaroid Medical Corp.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Polaroid Medical Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Polaroid Medical Corp. in the registry?
The most recently registered devices listed for Polaroid Medical Corp. include POLAROID HELIOS LASER IMAGER.