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FDA 510(k)

SIEMENS ORTHOPHOS DS/DS CEPH

K-Number: K972312 · 1997-09-15

ApplicantSiemens AG
Decision Date1997-09-15
Product CodeEHD
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

SIEMENS ORTHOPHOS DS/DS CEPH is the device name listed in this FDA 510(k) record. The listed applicant is Siemens AG. It received FDA 510(k) clearance on 1997-09-15 under 510(k) number K972312. The device is classified under product code EHD. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SIEMENS ORTHOPHOS DS/DS CEPH?

SIEMENS ORTHOPHOS DS/DS CEPH is a medical device that received FDA 510(k) clearance on 1997-09-15. The listed applicant is Siemens AG. The 510(k) number is K972312.

When did SIEMENS ORTHOPHOS DS/DS CEPH receive FDA 510(k) clearance?

SIEMENS ORTHOPHOS DS/DS CEPH received FDA 510(k) clearance on 1997-09-15, under 510(k) number K972312.

Who is the listed applicant for SIEMENS ORTHOPHOS DS/DS CEPH?

The FDA 510(k) record lists Siemens AG as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SIEMENS ORTHOPHOS DS/DS CEPH?

The FDA product code for SIEMENS ORTHOPHOS DS/DS CEPH is EHD.

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Other records listing Siemens AG as applicant

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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