D.Y. Instrument, Inc.
Country not established
- Devices
- 1
What D.Y. Instrument, Inc. makes
D.Y. Instrument, Inc. manufactures the AIS100 Automatic Intramuscular Stimulator, a device designed for electrical muscle stimulation therapy.
The AIS100 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
AIS100 Automatic Intramuscular Stimulator Ref K040580
510(k) 510(k)
Frequently asked questions
How many devices does D.Y. Instrument, Inc. have in the registry?
The registry currently lists 1 device for D.Y. Instrument, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list D.Y. Instrument, Inc.'s devices?
Among its 1 most recently registered device, D.Y. Instrument, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do D.Y. Instrument, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for D.Y. Instrument, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from D.Y. Instrument, Inc. in the registry?
The most recently registered devices listed for D.Y. Instrument, Inc. include AIS100 AUTOMATIC INTRAMUSCULAR STIMULATOR.