NRW

Stimulator, Intramuscular, Automatic

Product code
NRW
Device name
Stimulator, Intramuscular, Automatic
Device class
Class 2
21 CFR
21 CFR 880.5580
Medical specialty
General Hospital
Marketing pathway
510(K)
Flag
Third-party review eligible
510(k) clearances (last 3 years)
1

FDA classification definition

The Automatic Intramuscular Stimulator is a device that aids muscle stimulation by using a method called dry needling for treatment. The device consists of a main control unit, a hand-held motor unit, and an AC power supply adapter. The motor unit has a mounted disposal syringe and a needle mounting hardware for a disposable needle, and enables the practitioner to administer treatment with less physical effort. An EMG needle is used instead of an acupuncture needle because it is less flexible than the acupuncture needle

Definition text from the FDA device classification database (U.S. federal government work, public domain).

Official FDA classification page: NRW
Classification and pathway per current FDA publications. Data from openFDA (CC0).