|
Device | BIOSENSE WEBSTER CELSIUS FLTR CATHETER |
Generic Name | Cardiac ablation percutaneous catheter |
Applicant | Biosense Webster, Inc 31 Technology Drive Suite 200 Irvine, CA 92618 |
PMA Number | P950005 |
Supplement Number | S048 |
Date Received | 10/18/2013 |
Decision Date | 11/26/2013 |
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 THE OVEN PARAMETERS IN THE TIP REFLOW PROCESS AND IMPLEMENTATIONOF A NEW INSPECTION. |