ACOUSTIC RECORDER— 510(k) K943726

Name: FDA 510(k) clearance K943726
Creator: U.S. Food and Drug Administration
Published: 1994-11-30

Substantially Equivalent

Technology Applications Assoc., Inc.

FDA 510(k) clearance K943726 for ACOUSTIC RECORDER, Substantially Equivalent on 1994-11-30. Applicant: Technology Applications Assoc., Inc.. Device class: 1.

Clearance details

Applicant: Technology Applications Assoc., Inc.
Product code: Code DQC
Device class: Class 1
Regulation: 21 CFR 870.2390
Advisory panel: Cardiovascular
Date received: 1994-08-02
Decision date: 1994-11-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Diego, CA, US

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