Regulatory Strategies, Inc.
Country not established
- Devices
- 1
What Regulatory Strategies, Inc. makes
Regulatory Strategies, Inc. manufactures the ME 300 Muscle Tester, a device designed for assessing muscle strength and function, likely used in clinical or rehabilitation settings.
The ME 300 Muscle Tester is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Model Me 300 Muscle Tester Ref K943535
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Regulatory Strategies, Inc. have in the registry?
The registry currently lists 1 device for Regulatory Strategies, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Regulatory Strategies, Inc.'s devices?
Among its 1 most recently registered device, Regulatory Strategies, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Regulatory Strategies, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Regulatory Strategies, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Regulatory Strategies, Inc. in the registry?
The most recently registered devices listed for Regulatory Strategies, Inc. include MODEL ME 300 MUSCLE TESTER.