RFG-3CF— 510(k) K965182
Substantially EquivalentRadionics, Inc.
FDA 510(k) clearance K965182 for RFG-3CF, Substantially Equivalent on 1997-03-12. Applicant: Radionics, Inc..
Clearance details
- Applicant
- Radionics, Inc.
- Product code
- Code GXD
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Burlington, MA, US
Adverse events under product code GXD
product code GXD- Injury
- 228
- Total
- 228
Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →
Data sourced from openFDA. This site is unofficial and independent of the FDA.