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FDA 510(k)

KANTERON DICOM STATION (KDS), MODEL 3.0

K-Number: K073176 · 2008-03-19

ApplicantMonica Veytia
Decision Date2008-03-19
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

KANTERON DICOM STATION (KDS), MODEL 3.0 is the device name listed in this FDA 510(k) record. The listed applicant is Monica Veytia. It received FDA 510(k) clearance on 2008-03-19 under 510(k) number K073176. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KANTERON DICOM STATION (KDS), MODEL 3.0?

KANTERON DICOM STATION (KDS), MODEL 3.0 is a medical device that received FDA 510(k) clearance on 2008-03-19. The listed applicant is Monica Veytia. The 510(k) number is K073176.

When did KANTERON DICOM STATION (KDS), MODEL 3.0 receive FDA 510(k) clearance?

KANTERON DICOM STATION (KDS), MODEL 3.0 received FDA 510(k) clearance on 2008-03-19, under 510(k) number K073176.

Who is the listed applicant for KANTERON DICOM STATION (KDS), MODEL 3.0?

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

What is the FDA product code for KANTERON DICOM STATION (KDS), MODEL 3.0?

The FDA product code for KANTERON DICOM STATION (KDS), MODEL 3.0 is LLZ.

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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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