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FDA 510(k)

DENTAL X-RAY UNIT W/CEPHALOMETRIC ATTACH

K-Number: K781287 · 1978-09-11

ApplicantSiemens Corp.
Decision Date1978-09-11
Product CodeEAG
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

DENTAL X-RAY UNIT W/CEPHALOMETRIC ATTACH is the device name listed in this FDA 510(k) record. The listed applicant is Siemens Corp.. It received FDA 510(k) clearance on 1978-09-11 under 510(k) number K781287. The device is classified under product code EAG. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DENTAL X-RAY UNIT W/CEPHALOMETRIC ATTACH?

DENTAL X-RAY UNIT W/CEPHALOMETRIC ATTACH is a medical device that received FDA 510(k) clearance on 1978-09-11. The listed applicant is Siemens Corp.. The 510(k) number is K781287.

When did DENTAL X-RAY UNIT W/CEPHALOMETRIC ATTACH receive FDA 510(k) clearance?

DENTAL X-RAY UNIT W/CEPHALOMETRIC ATTACH received FDA 510(k) clearance on 1978-09-11, under 510(k) number K781287.

Who is the listed applicant for DENTAL X-RAY UNIT W/CEPHALOMETRIC ATTACH?

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

What is the FDA product code for DENTAL X-RAY UNIT W/CEPHALOMETRIC ATTACH?

The FDA product code for DENTAL X-RAY UNIT W/CEPHALOMETRIC ATTACH is EAG.

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Related Devices (Code: EAG)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K030699VERAVIEWEPOCS PANORAMIC/CEPHALOMETRIC X-RAY UNIT WITH CEPHALOMETRICJ. Morita Mfg. Corp.K021372VERAVIEWEPOCS PANORAMIC X-RAY UNIT WITH CEPHALOMETRIC CAPABILITYJ. Morita USA, Inc.K944162DENAR ACCUCEPH CEPHALOMETER IMAGING SYSTEMTeledyne Water PikK920189GX-C CEPHALOMETERGendex Corp.K896099DIGIGRAPH DIAGNOSTIC WORK/STATIONDolphin Imaging SystemsK870243BURNETT TMJ APPLIANCEMedrad, Inc.

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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