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FDA 510(k)

VERAVIEWEPOCS PANORAMIC/CEPHALOMETRIC X-RAY UNIT WITH CEPHALOMETRIC

K-Number: K030699 · 2003-05-29

ApplicantJ. Morita Mfg. Corp.
Decision Date2003-05-29
Product CodeEAG
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

VERAVIEWEPOCS PANORAMIC/CEPHALOMETRIC X-RAY UNIT WITH CEPHALOMETRIC is the device name listed in this FDA 510(k) record. The listed applicant is J. Morita Mfg. Corp.. It received FDA 510(k) clearance on 2003-05-29 under 510(k) number K030699. 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 VERAVIEWEPOCS PANORAMIC/CEPHALOMETRIC X-RAY UNIT WITH CEPHALOMETRIC?

VERAVIEWEPOCS PANORAMIC/CEPHALOMETRIC X-RAY UNIT WITH CEPHALOMETRIC is a medical device that received FDA 510(k) clearance on 2003-05-29. The listed applicant is J. Morita Mfg. Corp.. The 510(k) number is K030699.

When did VERAVIEWEPOCS PANORAMIC/CEPHALOMETRIC X-RAY UNIT WITH CEPHALOMETRIC receive FDA 510(k) clearance?

VERAVIEWEPOCS PANORAMIC/CEPHALOMETRIC X-RAY UNIT WITH CEPHALOMETRIC received FDA 510(k) clearance on 2003-05-29, under 510(k) number K030699.

Who is the listed applicant for VERAVIEWEPOCS PANORAMIC/CEPHALOMETRIC X-RAY UNIT WITH CEPHALOMETRIC?

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

What is the FDA product code for VERAVIEWEPOCS PANORAMIC/CEPHALOMETRIC X-RAY UNIT WITH CEPHALOMETRIC?

The FDA product code for VERAVIEWEPOCS PANORAMIC/CEPHALOMETRIC X-RAY UNIT WITH CEPHALOMETRIC 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.

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.K842463GX CEPHGendex Corp.

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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