The following data is part of a premarket notification filed by St. Jude Medical with the FDA for Brk Transseptal Needle.
| Device ID | K072278 |
| 510k Number | K072278 |
| Device Name: | BRK TRANSSEPTAL NEEDLE |
| Classification | Trocar |
| Applicant | ST. JUDE MEDICAL 14901 DEVEAU PL. Minnetonka, MN 55345 -2126 |
| Contact | Laura Moen-ftacek |
| Correspondent | Mark Job REGULATORY TECHNOLOGY SERVICES, LLC 1000 Westgate Drive, Suite 510k Saint Paul, MN 55114 |
| Product Code | DRC |
| CFR Regulation Number | 870.1390 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | Yes |
| Combination Product | No |
| Date Received | 2007-08-16 |
| Decision Date | 2007-09-13 |
| Summary: | summary |