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FDA 510(k)

ACOUSTIC RECORDER

K-Number: K943726 · 1994-11-30

ApplicantTechnology Applications Assoc., Inc.
Decision Date1994-11-30
Product CodeDQC
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ACOUSTIC RECORDER is the device name listed in this FDA 510(k) record. The listed applicant is Technology Applications Assoc., Inc.. It received FDA 510(k) clearance on 1994-11-30 under 510(k) number K943726. The device is classified under product code DQC. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACOUSTIC RECORDER?

ACOUSTIC RECORDER is a medical device that received FDA 510(k) clearance on 1994-11-30. The listed applicant is Technology Applications Assoc., Inc.. The 510(k) number is K943726.

When did ACOUSTIC RECORDER receive FDA 510(k) clearance?

ACOUSTIC RECORDER received FDA 510(k) clearance on 1994-11-30, under 510(k) number K943726.

Who is the listed applicant for ACOUSTIC RECORDER?

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

What is the FDA product code for ACOUSTIC RECORDER?

The FDA product code for ACOUSTIC RECORDER is DQC.

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Related Devices (Code: DQC)

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.

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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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