SIEMENS ORTHOPHOS DS/DS CEPH— 510(k) K972312
Substantially EquivalentSiemens AG
FDA 510(k) clearance K972312 for SIEMENS ORTHOPHOS DS/DS CEPH, Substantially Equivalent on 1997-09-15. Applicant: Siemens AG.
Clearance details
- Applicant
- Siemens AG
- Product code
- Code EHD
- Advisory panel
- Dental
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- North Attleboro, MA, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.