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FDA 510(k)

TA-6C - PART NUMBER SLZ 7520

K-Number: K860262 · 1986-04-23

ApplicantTeledyne Avionics Div. of Teledyne
Decision Date1986-04-23
Product CodeETY
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

TA-6C - PART NUMBER SLZ 7520 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 1986-04-23 under 510(k) number K860262. 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 TA-6C - PART NUMBER SLZ 7520?

TA-6C - PART NUMBER SLZ 7520 is a medical device that received FDA 510(k) clearance on 1986-04-23. The listed applicant is Teledyne Avionics Div. of Teledyne. The 510(k) number is K860262.

When did TA-6C - PART NUMBER SLZ 7520 receive FDA 510(k) clearance?

TA-6C - PART NUMBER SLZ 7520 received FDA 510(k) clearance on 1986-04-23, under 510(k) number K860262.

Who is the listed applicant for TA-6C - PART NUMBER SLZ 7520?

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-6C - PART NUMBER SLZ 7520?

The FDA product code for TA-6C - PART NUMBER SLZ 7520 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.

K860522SPIROMETER, MODEL TS-1000, PART NO. SLZ7504K855068SPIROMETER, MODEL TS-500 PART #SLZ7534K855069SPIROMETER TS-400 SLZ 7547K855070SPIROMETER MODEL TS-200 SLZ 7541K854043AUTOMATIC IMPEDANCE AUDIOMETER, TA-7BK851015TA-20 AUTOMATIC INDUSTIRAL AUDIOMETER

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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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