T-TECH DIGITAL, MODEL WL-22XXA SERIES

Device Classification Name

stimulator, nerve, transcutaneous, for pain relief

510(k) Number K033857
Device Name T-TECH DIGITAL, MODEL WL-22XXA SERIES
Applicant
WELL-LIFE HEALTHCARE, INC.
6c01, no.5, sec.5, hsin yi rd.
taipei, 

TW

106

Applicant Contact jenny hsiah
Correspondent
WELL-LIFE HEALTHCARE, INC.
6c01, no.5, sec.5, hsin yi rd.
taipei, 

TW

106

Correspodent Contact jenny hsiah
Regulation Number 882.5890
Classification Product Code
GZJ  
Subsequent Product Code
IPF  
Date Received 12/11/2003
Decision Date 12/19/2003
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

Neurology

510k Review Panel

Neurology

summary

summary

Type Special
Reviewed by Third Party No

Combination Product

No