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FDA 510(k)

AMPLAID 770 ADMITTANCE METER

K-Number: K903066 · 1990-10-24

ApplicantAmplus Corp.
Decision Date1990-10-24
Product CodeETY
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

AMPLAID 770 ADMITTANCE METER is the device name listed in this FDA 510(k) record. The listed applicant is Amplus Corp.. It received FDA 510(k) clearance on 1990-10-24 under 510(k) number K903066. 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 AMPLAID 770 ADMITTANCE METER?

AMPLAID 770 ADMITTANCE METER is a medical device that received FDA 510(k) clearance on 1990-10-24. The listed applicant is Amplus Corp.. The 510(k) number is K903066.

When did AMPLAID 770 ADMITTANCE METER receive FDA 510(k) clearance?

AMPLAID 770 ADMITTANCE METER received FDA 510(k) clearance on 1990-10-24, under 510(k) number K903066.

Who is the listed applicant for AMPLAID 770 ADMITTANCE METER?

The FDA 510(k) record lists Amplus Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AMPLAID 770 ADMITTANCE METER?

The FDA product code for AMPLAID 770 ADMITTANCE METER is ETY.

Related Clinical Trials

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Other records listing Amplus Corp. 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.

K891988AMPLAID A308 CLINICAL AUDIOMETERK884071AMPLAID EMG15K880059AMPLAID 309 CLINICAL AUDIOMETER

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

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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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