The following data is part of a premarket notification filed by Senorx, Inc. with the FDA for Contura Cavity Maintenance Catheter.
| Device ID | K092323 |
| 510k Number | K092323 |
| Device Name: | CONTURA CAVITY MAINTENANCE CATHETER |
| Classification | System, Applicator, Radionuclide, Remote-controlled |
| Applicant | SENORX, INC. 3 MORGAN Irvine, CA 92618 |
| 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 | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | Yes |
| Combination Product | No |
| Date Received | 2009-08-04 |
| Decision Date | 2009-08-19 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 15420045505261 | K092323 | 000 |