The following data is part of a premarket notification filed by Mercury Medical with the FDA for Mercury Medical Disposable Radiofrequency Cannula.
| Device ID | K000073 |
| 510k Number | K000073 |
| Device Name: | MERCURY MEDICAL DISPOSABLE RADIOFREQUENCY CANNULA |
| Classification | Probe, Radiofrequency Lesion |
| Applicant | MERCURY MEDICAL 160 SOUTH MAIN ST. SUITE A Middleton, MA 01949 |
| Contact | Matthew Nekoroski |
| Correspondent | Matthew Nekoroski MERCURY MEDICAL 160 SOUTH MAIN ST. SUITE A Middleton, MA 01949 |
| Product Code | GXI |
| CFR Regulation Number | 882.4725 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2000-01-10 |
| Decision Date | 2000-03-01 |