NEUROMED TS8 TEST STIMULATOR— 510(k) K903814
Substantially EquivalentNeuromed, Inc.
FDA 510(k) clearance K903814 for NEUROMED TS8 TEST STIMULATOR, Substantially Equivalent on 1991-01-16. Applicant: Neuromed, Inc..
Clearance details
- Applicant
- Neuromed, Inc.
- Product code
- Code GZB
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Ft. Lauderdale, FL, US
Adverse events under product code GZB
product code GZB- Death
- 4
- Injury
- 1,879
- Other
- 2
- Total
- 1,885
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.