PMA supplement
P950005 S009: CORDIS WEBSTER DIAGNOSTIC/ABLATION DEFLECTABLE TIP CATHETER
FDA PMA supplement · Normal 180 Day Track · Biosense Webster, Inc.
Key facts
| Original PMA | P950005 |
|---|---|
| Supplement number | S009 |
| Supplement type | Normal 180 Day Track |
| Reason for the supplement | Location Change - Manufacturer/Sterilizer/Packager/Supplier |
| Trade name | CORDIS WEBSTER DIAGNOSTIC/ABLATION DEFLECTABLE TIP CATHETER |
| Generic name | CATHETER, ELECTRODE RECORDING, OR PROBE, ELECTRODE RECORDING |
| Applicant | Biosense Webster, Inc. |
| Product code | DRF |
| Received date | Jul 31, 2000 |
| Decision date | Sep 29, 2000 |
At a glance
- No Expedited review granted
- No Approval order on file
- No Summary of safety and effectiveness on file
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About PMA supplements
A PMA supplement asks FDA to approve a change to a device that already holds a premarket approval: a new indication, a design or labeling change, a manufacturing site or process change.
Source: U.S. Food and Drug Administration (FDA), Premarket Approval (PMA) database · Source date: