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FDA 510(k)

ODONTOSON 3

K-Number: K782133 · 1979-02-27

ApplicantMdt Corp., Inc.
Decision Date1979-02-27
Product CodeELC
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ODONTOSON 3 is the device name listed in this FDA 510(k) record. The listed applicant is Mdt Corp., Inc.. It received FDA 510(k) clearance on 1979-02-27 under 510(k) number K782133. The device is classified under product code ELC. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ODONTOSON 3?

ODONTOSON 3 is a medical device that received FDA 510(k) clearance on 1979-02-27. The listed applicant is Mdt Corp., Inc.. The 510(k) number is K782133.

When did ODONTOSON 3 receive FDA 510(k) clearance?

ODONTOSON 3 received FDA 510(k) clearance on 1979-02-27, under 510(k) number K782133.

Who is the listed applicant for ODONTOSON 3?

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

What is the FDA product code for ODONTOSON 3?

The FDA product code for ODONTOSON 3 is ELC.

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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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