|
Device | SAFIRE CARDIAC ABLATION SYSTEM |
Generic Name | Cardiac ablation percutaneous catheter |
Applicant | St. Jude Medical 14900 MINNETONKA IND RD MINNETONKA, MN 55345 |
PMA Number | P960016 |
Supplement Number | S025 |
Date Received | 10/28/2009 |
Decision Date | 11/20/2009 |
Product Code |
LPB |
Advisory Committee |
Cardiovascular |
Supplement Type | 30-Day Notice |
Supplement Reason | Process Change - Manufacturer/Sterilizer/Packager/Supplier |
Expedited Review Granted? | No |
Combination Product | No |
Approval Order Statement CHANGE TO AN AUTOMATED MANUFACTURING PROCESS, A CHANGE IN A WELDING PROCESS AND A CHANGE TO PROCESS MONITORING TESTING. |