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FDA 510(k)

SELF-RECORDING ADMITTANCE METER 709

K-Number: K802097 · 1980-10-10

ApplicantAmplaid USA, Inc.
Decision Date1980-10-10
Product CodeETY
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

SELF-RECORDING ADMITTANCE METER 709 is the device name listed in this FDA 510(k) record. The listed applicant is Amplaid USA, Inc.. It received FDA 510(k) clearance on 1980-10-10 under 510(k) number K802097. 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 SELF-RECORDING ADMITTANCE METER 709?

SELF-RECORDING ADMITTANCE METER 709 is a medical device that received FDA 510(k) clearance on 1980-10-10. The listed applicant is Amplaid USA, Inc.. The 510(k) number is K802097.

When did SELF-RECORDING ADMITTANCE METER 709 receive FDA 510(k) clearance?

SELF-RECORDING ADMITTANCE METER 709 received FDA 510(k) clearance on 1980-10-10, under 510(k) number K802097.

Who is the listed applicant for SELF-RECORDING ADMITTANCE METER 709?

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

What is the FDA product code for SELF-RECORDING ADMITTANCE METER 709?

The FDA product code for SELF-RECORDING ADMITTANCE METER 709 is ETY.

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Other records listing Amplaid USA, Inc. 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.

K861014AMPLAID MK15 (EVOKED POTENTIAL SYSTEM)K832510EVOKED POTENTIALS SYSTEM MK10K810482SOMATOSENSORY STIMULATORK810473MK6 ERA SYSTEMK810481VISUAL PATTERN REVERSAL GEN. & PHOTIC S.K802963101, 151, 161 PORTABLE AUDIOMETERS

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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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