TENS PRO 900


Device Classification Name

stimulator, nerve, transcutaneous, for pain relief

510(k) Number K023726
Device Name TENS PRO 900
Original Applicant
ACUMED MEDICAL SUPPLIES, LTD.
1151 hope st.
stanford, 
CT 
06907

Original Contact richard keen
Regulation Number 882.5890
Classification Product Code
GZJ  
Date Received 11/06/2002
Decision Date 06/17/2003
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

Neurology

510k Review Panel

Neurology

statement

statement

Type Traditional
Reviewed by Third Party No

Combination Product

No