BWJ — Locator, Acupuncture Point Class II

FDA Device Classification

FDA product code BWJ covers "Locator, Acupuncture Point", a Class II medical device regulated under 21 CFR 880.5580. Submissions are reviewed by the General Hospital panel. At least 3 recent 510(k) clearances have been granted under this product code.

Classification Details

Product Code
BWJ
Device Class
Class II
Regulation Number
880.5580
Submission Type
Review Panel
HO
Medical Specialty
General Hospital
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K792501staodynamicsPLS MINIFebruary 26, 1980
K792529staodynamicsPOINT LOCATOR STIMULATORFebruary 26, 1980
K772424erconaRYUSEIMay 9, 1978