BAYLIS PAIN MANAGEMENT PROBE/PMP-20-145 AND BAYLIS PAIN MANAGEMENT CONNECTOR CABLE/PMX-BAY-BAY


codes

Device Classification Name

probe, radiofrequency lesion

510(k) Number K002389
Device Name BAYLIS PAIN MANAGEMENT PROBE/PMP-20-145 AND BAYLIS PAIN MANAGEMENT CONNECTOR CABLE/PMX-BAY-BAY
Original Applicant
BAYLIS MEDICAL CO., INC.
5160 explorer drive, unit 5
mississauga, 

CA

l4w-4t7

Original Contact kris shah
Regulation Number 882.4725
Classification Product Code
GXI  
Date Received 08/04/2000
Decision Date 10/23/2000
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

Neurology

510k Review Panel

Neurology

Type Traditional
Reviewed by Third Party No

Combination Product

No