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 |
Applicant |
BAYLIS MEDICAL CO., INC. |
5160 EXPLORER DRIVE, UNIT 5 |
MISSISSAUGA,
CA
L4W-4T7
|
|
Applicant Contact |
KRIS SHAH |
Correspondent |
BAYLIS MEDICAL CO., INC. |
5160 EXPLORER DRIVE, UNIT 5 |
MISSISSAUGA,
CA
L4W-4T7
|
|
Correspondent Contact |
KRIS SHAH |
Regulation Number | 882.4725
|
Classification Product Code |
|
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
|
|
|