The following data is part of a premarket notification filed by Senorx, Inc. with the FDA for Senorad Multi-lumen Balloon Source Applicator For Branchytherapy.
| Device ID | K071229 |
| 510k Number | K071229 |
| Device Name: | SENORAD MULTI-LUMEN BALLOON SOURCE APPLICATOR FOR BRANCHYTHERAPY |
| Classification | System, Applicator, Radionuclide, Remote-controlled |
| Applicant | SENORX, INC. 11 COLUMBIA Aliso Viejo, CA 92656 |
| Contact | Eben Gordon |
| Correspondent | Mark Job REGULATORY TECHNOLOGY SERVICES, LLC 1000 Westgate Drive, Suite 510k Saint Paul, MN 55114 |
| Product Code | JAQ |
| CFR Regulation Number | 892.5700 [🔎] |
| Decision | Se - With Limitations (SESU) |
| Type | Traditional |
| 3rd Party Reviewed | Yes |
| Combination Product | No |
| Date Received | 2007-05-03 |
| Decision Date | 2007-05-18 |
| Summary: | summary |