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FDA 510(k)

ACOUSTIC ANALYZER AA30

K-Number: K930260 · 1993-07-13

ApplicantPrecision Acoustics Ind., Inc.
Decision Date1993-07-13
Product CodeEWO
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

ACOUSTIC ANALYZER AA30 is the device name listed in this FDA 510(k) record. The listed applicant is Precision Acoustics Ind., Inc.. It received FDA 510(k) clearance on 1993-07-13 under 510(k) number K930260. The device is classified under product code EWO. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACOUSTIC ANALYZER AA30?

ACOUSTIC ANALYZER AA30 is a medical device that received FDA 510(k) clearance on 1993-07-13. The listed applicant is Precision Acoustics Ind., Inc.. The 510(k) number is K930260.

When did ACOUSTIC ANALYZER AA30 receive FDA 510(k) clearance?

ACOUSTIC ANALYZER AA30 received FDA 510(k) clearance on 1993-07-13, under 510(k) number K930260.

Who is the listed applicant for ACOUSTIC ANALYZER AA30?

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

What is the FDA product code for ACOUSTIC ANALYZER AA30?

The FDA product code for ACOUSTIC ANALYZER AA30 is EWO.

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Other records listing Precision Acoustics Ind., Inc. as applicant

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Related Devices (Code: EWO)

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.

K234095OtoNova/OtoNova ProOtodynamicsK240430Otoport ProOtodynamics, Ltd.K231545hearOAEHearx SA (Pty) , Ltd.K213345Sentiero, AuDX, AuDX PRO, Sentiero Desktop, AuDX PRO Flex, Sentiero Advanced, NavPRO ONEPath Medical GmbHK191372LyraInteracoustics A/SK180287GSI CortiGrason-Stadler, Inc.

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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