FDA 510(k)

DIGIDENT ELEKTRONIC APEX LOCATOR

K-Number: K832118 · 1983-09-26

Decision Date1983-09-26

Product Code

DecisionSubstantially Equivalent

Device Summary

DIGIDENT ELEKTRONIC APEX LOCATOR is the device name listed in this FDA 510(k) record. The listed applicant is Ora-Muszeripari Szovetkezet. It received FDA 510(k) clearance on 1983-09-26 under 510(k) number K832118. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DIGIDENT ELEKTRONIC APEX LOCATOR?

DIGIDENT ELEKTRONIC APEX LOCATOR is a medical device that received FDA 510(k) clearance on 1983-09-26. The listed applicant is Ora-Muszeripari Szovetkezet. The 510(k) number is K832118.

When did DIGIDENT ELEKTRONIC APEX LOCATOR receive FDA 510(k) clearance?

DIGIDENT ELEKTRONIC APEX LOCATOR received FDA 510(k) clearance on 1983-09-26, under 510(k) number K832118.

Who is the listed applicant for DIGIDENT ELEKTRONIC APEX LOCATOR?

The FDA 510(k) record lists Ora-Muszeripari Szovetkezet as the applicant. This does not by itself establish the device manufacturer.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.