The following data is part of a premarket notification filed by Biosense Webster, Inc. with the FDA for Carto Xp Ep Navigation System, Version 9.
| Device ID | K070240 |
| 510k Number | K070240 |
| Device Name: | CARTO XP EP NAVIGATION SYSTEM, VERSION 9 |
| Classification | Computer, Diagnostic, Programmable |
| Applicant | BIOSENSE WEBSTER, INC. 3333 DIAMOND CANYON RD. Diamond Bar, CA 91765 |
| Contact | Neelu Medhekar |
| Correspondent | Neelu Medhekar BIOSENSE WEBSTER, INC. 3333 DIAMOND CANYON RD. Diamond Bar, CA 91765 |
| Product Code | DQK |
| CFR Regulation Number | 870.1425 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2007-01-25 |
| Decision Date | 2007-05-04 |
| Summary: | summary |