GEODESIC PHOTOGRAMMETRY SYSTEM
FDA 510(k) clearance K043309 · decided 2005-01-26
Clearance details
- K-number
- K043309
- Device name
- GEODESIC PHOTOGRAMMETRY SYSTEM
- Applicant
- Electrical Geodesics, Incorporated
- Decision
- Substantially Equivalent
- Date received
- 2004-12-01
- Decision date
- 2005-01-26
- Days to decision
- 56 days
- Clearance type
- Traditional
- Product code
- GWQ
- Device class
- 2
- Regulation number
- 882.1400
- Medical specialty
- Neurology
- Advisory committee
- Neurology
- Location
- Eugene, OR, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.