The following data is part of a premarket notification filed by Senorx, Inc. with the FDA for Senosonix Ultrasound Breast Biopsy System.
| Device ID | K072541 |
| 510k Number | K072541 |
| Device Name: | SENOSONIX ULTRASOUND BREAST BIOPSY SYSTEM |
| Classification | Transducer, Ultrasonic, Diagnostic |
| Applicant | SENORX, INC. 11 COLUMBIA Aliso Viejo, CA 92656 |
| Correspondent | Mark Job REGULATORY TECHNOLOGY SERVICES, LLC 1000 Westgate Drive, Suite 510k Saint Paul, MN 55114 |
| Product Code | ITX |
| Subsequent Product Code | IYN |
| Subsequent Product Code | IYO |
| Subsequent Product Code | KNW |
| CFR Regulation Number | 892.1570 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | Yes |
| Combination Product | No |
| Date Received | 2007-09-10 |
| Decision Date | 2007-09-25 |
| Summary: | summary |