NEUROSCOPE SEEG
FDA 510(k) clearance K861884 · decided 1986-10-14
Clearance details
- K-number
- K861884
- Device name
- NEUROSCOPE SEEG
- Applicant
- Siegen Corp.
- Decision
- Substantially Equivalent
- Date received
- 1986-05-15
- Decision date
- 1986-10-14
- Days to decision
- 152 days
- Clearance type
- Traditional
- Product code
- GWO
- Device class
- 2
- Regulation number
- 882.5320
- Medical specialty
- Neurology
- Advisory committee
- Neurology
- Location
- Mountain View, CA, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.