LD-I 75 AND LD-I 200


Device Classification Name

powered light based non-laser non-thermal instrument with non-heating effect for adjunctive use in pain therapy

510(k) Number K072551
Device Name LD-I 75 AND LD-I 200
Applicant
MEDITECH INTERNATIONAL, INC.
1151 hope st.
stamford, 
CT 
06907

Applicant Contact richard keen
Correspondent
MEDITECH INTERNATIONAL, INC.
1151 hope st.
stamford, 
CT 
06907

Correspodent Contact richard keen
Regulation Number 890.5500
Classification Product Code
NHN  
Date Received 09/10/2007
Decision Date 04/02/2008
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

Physical Medicine

510k Review Panel

General & Plastic Surgery

summary

summary

Type Traditional
Reviewed by Third Party No

Combination Product

No