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FDA 510(k)

ANMP (ACOUSTIC NEURO MODULATION PROTOCOL)

K-Number: K030791 · 2003-04-17

Decision Date2003-04-17
Product CodeKLW
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

ANMP (ACOUSTIC NEURO MODULATION PROTOCOL) is the device name listed in this FDA 510(k) record. The listed applicant is Tinnitech, Ltd.. It received FDA 510(k) clearance on 2003-04-17 under 510(k) number K030791. The device is classified under product code KLW. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

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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