THE LEADAWAY


Device Classification Name

cable, electrode

510(k) Number K992372
Device Name THE LEADAWAY
Applicant
THERAPY EQUIPMENT, INC.
13860 wellington trace, #310
west palm beach, 
FL 
33414

Applicant Contact glenn buchan
Correspondent
THERAPY EQUIPMENT, INC.
13860 wellington trace, #310
west palm beach, 
FL 
33414

Correspodent Contact glenn buchan
Regulation Number 890.1175
Classification Product Code
IKD  
Date Received 07/15/1999
Decision Date 10/13/1999
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

Physical Medicine

510k Review Panel

Neurology

statement

statement

Type Traditional
Reviewed by Third Party No

Combination Product

No