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FDA 510(k)

AUTOMATIC TYMPANOMETER

K-Number: K923073 · 1993-02-19

ApplicantLife-Tech Intl., Inc.
Decision Date1993-02-19
Product CodeETY
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

AUTOMATIC TYMPANOMETER is the device name listed in this FDA 510(k) record. The listed applicant is Life-Tech Intl., Inc.. It received FDA 510(k) clearance on 1993-02-19 under 510(k) number K923073. 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 AUTOMATIC TYMPANOMETER?

AUTOMATIC TYMPANOMETER is a medical device that received FDA 510(k) clearance on 1993-02-19. The listed applicant is Life-Tech Intl., Inc.. The 510(k) number is K923073.

When did AUTOMATIC TYMPANOMETER receive FDA 510(k) clearance?

AUTOMATIC TYMPANOMETER received FDA 510(k) clearance on 1993-02-19, under 510(k) number K923073.

Who is the listed applicant for AUTOMATIC TYMPANOMETER?

The FDA 510(k) record lists Life-Tech Intl., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AUTOMATIC TYMPANOMETER?

The FDA product code for AUTOMATIC TYMPANOMETER is ETY.

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Other records listing Life-Tech Intl., Inc. as applicant

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Related Devices (Code: ETY)

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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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