NEUROSOFT'S SOURCE
FDA 510(k) clearance K011241 · decided 2001-09-19
Clearance details
- K-number
- K011241
- Device name
- NEUROSOFT'S SOURCE
- Applicant
- Neurosoft, Inc.
- Decision
- Substantially Equivalent
- Date received
- 2001-04-23
- Decision date
- 2001-09-19
- Days to decision
- 149 days
- Clearance type
- Traditional
- Product code
- OLX
- Device class
- 2
- Regulation number
- 882.1400
- Medical specialty
- Neurology
- Advisory committee
- Neurology
- Location
- El Paso, TX, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.