MERCURY MEDICAL DISPOSABLE RADIOFREQUENCY CANNULA
FDA 510(k) clearance K000073 · decided 2000-03-01
Clearance details
- K-number
- K000073
- Device name
- MERCURY MEDICAL DISPOSABLE RADIOFREQUENCY CANNULA
- Applicant
- Mercury Medical
- Decision
- Substantially Equivalent
- Date received
- 2000-01-10
- Decision date
- 2000-03-01
- Days to decision
- 51 days
- Clearance type
- Traditional
- Product code
- GXI
- Device class
- 2
- Regulation number
- 882.4725
- Medical specialty
- Neurology
- Advisory committee
- Neurology
- Location
- Middleton, MA, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
| Record | Firm | Date |
|---|---|---|
| Neurotherm Curved Radiofrequency (RF) cannnula 10 cm 18 gauge, 10 mm active tip Model Numb recall (Z-1247-2016) | Neurotherm, Inc. | 2016-03-24 |