ANMP (ACOUSTIC NEURO MODULATION PROTOCOL)— 510(k) K030791

Name: FDA 510(k) clearance K030791
Creator: U.S. Food and Drug Administration
Published: 2003-04-17

Substantially Equivalent

Tinnitech, Ltd.

FDA 510(k) clearance K030791 for ANMP (ACOUSTIC NEURO MODULATION PROTOCOL), Substantially Equivalent on 2003-04-17. Applicant: Tinnitech, Ltd.. Device class: 2.

Clearance details

Applicant: Tinnitech, Ltd.
Product code: Code KLW
Device class: Class 2
Regulation: 21 CFR 874.3400
Advisory panel: Ear, Nose, Throat
Date received: 2003-03-12
Decision date: 2003-04-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Sydney, AU

Download summary PDF View on FDA.gov ↗

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