The following data is part of a premarket notification filed by Confirma, Inc. with the FDA for Confirma Breast Mri Interventional Components.
| Device ID | K071534 |
| 510k Number | K071534 |
| Device Name: | CONFIRMA BREAST MRI INTERVENTIONAL COMPONENTS |
| Classification | Coil, Magnetic Resonance, Specialty |
| Applicant | CONFIRMA, INC. 11040 MAIN STREET SUITE 100 Bellevue, WA 98004 |
| Contact | Patricia A Milbank |
| Correspondent | Patricia A Milbank CONFIRMA, INC. 11040 MAIN STREET SUITE 100 Bellevue, WA 98004 |
| Product Code | MOS |
| CFR Regulation Number | 892.1000 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2007-06-05 |
| Decision Date | 2007-07-09 |
| Summary: | summary |