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FDA 510(k)

MVS-MODEL SEU-6, DEU-6

K-Number: K781488 · 1978-09-27

ApplicantDentsply Intl.
Decision Date1978-09-27
Product CodeEHZ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

MVS-MODEL SEU-6, DEU-6 is the device name listed in this FDA 510(k) record. The listed applicant is Dentsply Intl.. It received FDA 510(k) clearance on 1978-09-27 under 510(k) number K781488. 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-MODEL SEU-6, DEU-6?

MVS-MODEL SEU-6, DEU-6 is a medical device that received FDA 510(k) clearance on 1978-09-27. The listed applicant is Dentsply Intl.. The 510(k) number is K781488.

When did MVS-MODEL SEU-6, DEU-6 receive FDA 510(k) clearance?

MVS-MODEL SEU-6, DEU-6 received FDA 510(k) clearance on 1978-09-27, under 510(k) number K781488.

Who is the listed applicant for MVS-MODEL SEU-6, DEU-6?

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-MODEL SEU-6, DEU-6?

The FDA product code for MVS-MODEL SEU-6, DEU-6 is 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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