STOCKERT NEURO N50, MODEL12267
FDA 510(k) clearance K070336 · decided 2007-06-14
Clearance details
- K-number
- K070336
- Device name
- STOCKERT NEURO N50, MODEL12267
- Applicant
- Stockert GmbH
- Decision
- Substantially Equivalent
- Date received
- 2007-02-05
- Decision date
- 2007-06-14
- Days to decision
- 129 days
- Clearance type
- Traditional
- Product code
- GXD
- Device class
- 2
- Regulation number
- 882.4400
- Medical specialty
- Neurology
- Advisory committee
- Neurology
- Location
- Freiburg, B-W, DE
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.