PAJUNKS STIMULONG TSUI-METHOD SET
FDA 510(k) clearance K062900 · decided 2007-01-12
Clearance details
- K-number
- K062900
- Device name
- PAJUNKS STIMULONG TSUI-METHOD SET
- Applicant
- PAJUNK GmbH Medizintechnologie
- Decision
- Substantially Equivalent
- Date received
- 2006-09-27
- Decision date
- 2007-01-12
- Days to decision
- 107 days
- Clearance type
- Traditional
- Product code
- CAZ
- Device class
- 2
- Regulation number
- 868.5140
- Medical specialty
- Anesthesiology
- Advisory committee
- Anesthesiology
- Location
- Geisingen, DE
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.