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FDA 510(k)

WILSON EUSTACHIAN TUBAL, SONOGRAPH

K-Number: K823774 · 1983-01-17

ApplicantAntares Technical Associates, Inc.
Decision Date1983-01-17
Product CodeETK
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

WILSON EUSTACHIAN TUBAL, SONOGRAPH is the device name listed in this FDA 510(k) record. The listed applicant is Antares Technical Associates, Inc.. It received FDA 510(k) clearance on 1983-01-17 under 510(k) number K823774. The device is classified under product code ETK. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WILSON EUSTACHIAN TUBAL, SONOGRAPH?

WILSON EUSTACHIAN TUBAL, SONOGRAPH is a medical device that received FDA 510(k) clearance on 1983-01-17. The listed applicant is Antares Technical Associates, Inc.. The 510(k) number is K823774.

When did WILSON EUSTACHIAN TUBAL, SONOGRAPH receive FDA 510(k) clearance?

WILSON EUSTACHIAN TUBAL, SONOGRAPH received FDA 510(k) clearance on 1983-01-17, under 510(k) number K823774.

Who is the listed applicant for WILSON EUSTACHIAN TUBAL, SONOGRAPH?

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

What is the FDA product code for WILSON EUSTACHIAN TUBAL, SONOGRAPH?

The FDA product code for WILSON EUSTACHIAN TUBAL, SONOGRAPH is ETK.

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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.

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