The following data is part of a premarket notification filed by Biosense Webster, Inc. with the FDA for Carto 3 Version 1.05 Ep Navigation System And Accessories.
| Device ID | K093455 |
| 510k Number | K093455 |
| Device Name: | CARTO 3 VERSION 1.05 EP NAVIGATION SYSTEM AND ACCESSORIES |
| Classification | Computer, Diagnostic, Programmable |
| Applicant | BIOSENSE WEBSTER, INC. 3333 DIAMOND CANYON RD. Diamond Bar, CA 91765 |
| Contact | Balaka Das |
| Correspondent | Balaka Das BIOSENSE WEBSTER, INC. 3333 DIAMOND CANYON RD. Diamond Bar, CA 91765 |
| Product Code | DQK |
| CFR Regulation Number | 870.1425 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2009-11-05 |
| Decision Date | 2009-12-04 |
| Summary: | summary |