ANMP (ACOUSTIC NEURO MODULATION PROTOCOL)
K-Number: K030791 · 2003-04-17
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Device Summary
Frequently Asked Questions
What is the ANMP (ACOUSTIC NEURO MODULATION PROTOCOL)?
ANMP (ACOUSTIC NEURO MODULATION PROTOCOL) is a medical device that received FDA 510(k) clearance on 2003-04-17. The listed applicant is Tinnitech, Ltd.. The 510(k) number is K030791.
When did ANMP (ACOUSTIC NEURO MODULATION PROTOCOL) receive FDA 510(k) clearance?
ANMP (ACOUSTIC NEURO MODULATION PROTOCOL) received FDA 510(k) clearance on 2003-04-17, under 510(k) number K030791.
Who is the listed applicant for ANMP (ACOUSTIC NEURO MODULATION PROTOCOL)?
The FDA 510(k) record lists Tinnitech, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ANMP (ACOUSTIC NEURO MODULATION PROTOCOL)?
The FDA product code for ANMP (ACOUSTIC NEURO MODULATION PROTOCOL) is KLW.
Related Clinical Trials
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.
Related Devices (Code: KLW)
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.
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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