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FDA 510(k)

TA-20 AUTOMATIC INDUSTIRAL AUDIOMETER

K-Number: K851015 · 1985-06-04

Decision Date1985-06-04
Product CodeEWO
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

TA-20 AUTOMATIC INDUSTIRAL AUDIOMETER is the device name listed in this FDA 510(k) record. The listed applicant is Teledyne Avionics Div. of Teledyne. It received FDA 510(k) clearance on 1985-06-04 under 510(k) number K851015. The device is classified under product code EWO. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TA-20 AUTOMATIC INDUSTIRAL AUDIOMETER?

TA-20 AUTOMATIC INDUSTIRAL AUDIOMETER is a medical device that received FDA 510(k) clearance on 1985-06-04. The listed applicant is Teledyne Avionics Div. of Teledyne. The 510(k) number is K851015.

When did TA-20 AUTOMATIC INDUSTIRAL AUDIOMETER receive FDA 510(k) clearance?

TA-20 AUTOMATIC INDUSTIRAL AUDIOMETER received FDA 510(k) clearance on 1985-06-04, under 510(k) number K851015.

Who is the listed applicant for TA-20 AUTOMATIC INDUSTIRAL AUDIOMETER?

The FDA 510(k) record lists Teledyne Avionics Div. of Teledyne as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TA-20 AUTOMATIC INDUSTIRAL AUDIOMETER?

The FDA product code for TA-20 AUTOMATIC INDUSTIRAL AUDIOMETER is EWO.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Teledyne Avionics Div. of Teledyne as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 13 devices →

Related Devices (Code: EWO)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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