|
Device | Maestro 4000 Controller |
Generic Name | Cardiac ablation percutaneous catheter |
Applicant | Boston Scientific Corp. 150 BAYTECH DRIVE SAN JOSE, CA 95134 |
PMA Number | P920047 |
Supplement Number | S110 |
Date Received | 06/21/2018 |
Decision Date | 01/28/2019 |
Product Code |
LPB |
Advisory Committee |
Cardiovascular |
Supplement Type | Normal 180 Day Track |
Supplement Reason | Change Design/Components/Specifications/Material |
Expedited Review Granted? | No |
Combination Product | No |
Approval Order Statement Approval to update the firmware/software of the Maestro 4000 Controller from version 5.14 to version 5.23 and the MetriQ Pump version 0.0.64 to version 1.1. |