Allegheny Plastics, Inc.
Country not established
- Devices
- 1
What Allegheny Plastics, Inc. makes
Allegheny Plastics, Inc. manufactures the RULE, PUPILLARY device, which is a medical device used for pupil assessment.
The company's products are listed in the FDA 510(k) registry and are classified as Class I medical devices. Allegheny Plastics, Inc. is based in the US.
Catalogue
Rule, Pupillary Ref K873440
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Allegheny Plastics, Inc. have in the registry?
The registry currently lists 1 device for Allegheny Plastics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Allegheny Plastics, Inc.'s devices?
Among its 1 most recently registered device, Allegheny Plastics, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Allegheny Plastics, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Allegheny Plastics, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Allegheny Plastics, Inc. in the registry?
The most recently registered devices listed for Allegheny Plastics, Inc. include RULE, PUPILLARY.