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FDA 510(k)

AUTO-TACH

K-Number: K832291 · 1983-08-31

ApplicantDentsply Intl.
Decision Date1983-08-31
Product CodeDYH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

AUTO-TACH is the device name listed in this FDA 510(k) record. The listed applicant is Dentsply Intl.. It received FDA 510(k) clearance on 1983-08-31 under 510(k) number K832291. The device is classified under product code DYH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AUTO-TACH?

AUTO-TACH is a medical device that received FDA 510(k) clearance on 1983-08-31. The listed applicant is Dentsply Intl.. The 510(k) number is K832291.

When did AUTO-TACH receive FDA 510(k) clearance?

AUTO-TACH received FDA 510(k) clearance on 1983-08-31, under 510(k) number K832291.

Who is the listed applicant for AUTO-TACH?

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 AUTO-TACH?

The FDA product code for AUTO-TACH is DYH.

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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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