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FDA 510(k)

MVS UNIT, MODEL SEU-8 AND DEU-8, 80

K-Number: K782068 · 1979-01-26

ApplicantDentsply Intl.
Decision Date1979-01-26
Product CodeEHZ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

MVS UNIT, MODEL SEU-8 AND DEU-8, 80 is the device name listed in this FDA 510(k) record. The listed applicant is Dentsply Intl.. It received FDA 510(k) clearance on 1979-01-26 under 510(k) number K782068. The device is classified under product code EHZ. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MVS UNIT, MODEL SEU-8 AND DEU-8, 80?

MVS UNIT, MODEL SEU-8 AND DEU-8, 80 is a medical device that received FDA 510(k) clearance on 1979-01-26. The listed applicant is Dentsply Intl.. The 510(k) number is K782068.

When did MVS UNIT, MODEL SEU-8 AND DEU-8, 80 receive FDA 510(k) clearance?

MVS UNIT, MODEL SEU-8 AND DEU-8, 80 received FDA 510(k) clearance on 1979-01-26, under 510(k) number K782068.

Who is the listed applicant for MVS UNIT, MODEL SEU-8 AND DEU-8, 80?

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

What is the FDA product code for MVS UNIT, MODEL SEU-8 AND DEU-8, 80?

The FDA product code for MVS UNIT, MODEL SEU-8 AND DEU-8, 80 is EHZ.

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Related Devices (Code: EHZ)

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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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