DUOMED, SERIES 500, (MODELS ID 500, FL 500)


Device Classification Name

stimulator, nerve, transcutaneous, for pain relief

510(k) Number K030140
Device Name DUOMED, SERIES 500, (MODELS ID 500, FL 500)
Original Applicant
DUOMED INC.
400 northpoint parkway #406
west palm beach, 
FL 
33407

Original Contact charles kokinos
Regulation Number 882.5890
Classification Product Code
GZJ  
Date Received 01/14/2003
Decision Date 03/18/2003
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

Neurology

510k Review Panel

Neurology

summary

summary

Type Traditional
Reviewed by Third Party No

Combination Product

No