SMITHWICK CAROTID SHUNT
FDA 510(k) clearance K062474 · decided 2006-11-09
Clearance details
- K-number
- K062474
- Device name
- SMITHWICK CAROTID SHUNT
- Applicant
- Mcpherson Enterprises, Inc.
- Decision
- Substantially Equivalent
- Date received
- 2006-08-24
- Decision date
- 2006-11-09
- Days to decision
- 77 days
- Clearance type
- Traditional
- Product code
- DXC
- Device class
- 2
- Regulation number
- 870.4450
- Medical specialty
- Cardiovascular
- Advisory committee
- Cardiovascular
- Location
- Pinellas Park, FL, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.