SIEMENS ORTHOPHOS DS/DS CEPH— 510(k) K972312

Substantially Equivalent

Siemens AG

FDA 510(k) clearance K972312 for SIEMENS ORTHOPHOS DS/DS CEPH, Substantially Equivalent on 1997-09-15. Applicant: Siemens AG. Device class: 2.

Clearance details

Applicant: Siemens AG
Product code: Code EHD
Device class: Class 2
Regulation: 21 CFR 872.1800
Advisory panel: Dental
Date received: 1997-06-20
Decision date: 1997-09-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: North Attleboro, MA, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.