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FDA 510(k)

AUTO-TYMPANIGRAPH (TA-5A)

K-Number: K811509 · 1981-06-16

ApplicantTeledyne Avionics Div. of Teledyne
Decision Date1981-06-16
Product CodeETY
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

AUTO-TYMPANIGRAPH (TA-5A) 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 1981-06-16 under 510(k) number K811509. The device is classified under product code ETY. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AUTO-TYMPANIGRAPH (TA-5A)?

AUTO-TYMPANIGRAPH (TA-5A) is a medical device that received FDA 510(k) clearance on 1981-06-16. The listed applicant is Teledyne Avionics Div. of Teledyne. The 510(k) number is K811509.

When did AUTO-TYMPANIGRAPH (TA-5A) receive FDA 510(k) clearance?

AUTO-TYMPANIGRAPH (TA-5A) received FDA 510(k) clearance on 1981-06-16, under 510(k) number K811509.

Who is the listed applicant for AUTO-TYMPANIGRAPH (TA-5A)?

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 AUTO-TYMPANIGRAPH (TA-5A)?

The FDA product code for AUTO-TYMPANIGRAPH (TA-5A) is ETY.

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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.

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Related Devices (Code: ETY)

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.

K183201Hearing Healthcare ProDb Diagnostic Systems, Inc.K171038Hearing Healthcare ProDb Diagnostic Systems, Inc.K162210touchTympMaico Diagnostics GmbHK161707Madsen ZodiacGn OtometricsK121847TITANInteracoustics A/SK083861TITAN, TITAN SHOULDER BOX, TITAN CRADLE, TITAN PRINTER, TITAN IMP440, IMP440 MODULE, TITAN SUITEInteracoustics AS

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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