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FDA 510(k)

MYOHEALTH CLENCHING INHIBITOR

K-Number: K040315 · 2004-08-27

Decision Date2004-08-27
Product CodeMQC
DecisionSubstantially Equivalent

Device Summary

MYOHEALTH CLENCHING INHIBITOR is the device name listed in this FDA 510(k) record. The listed applicant is Mci-Myohealth Systems. It received FDA 510(k) clearance on 2004-08-27 under 510(k) number K040315. The device is classified under product code MQC. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MYOHEALTH CLENCHING INHIBITOR?

MYOHEALTH CLENCHING INHIBITOR is a medical device that received FDA 510(k) clearance on 2004-08-27. The listed applicant is Mci-Myohealth Systems. The 510(k) number is K040315.

When did MYOHEALTH CLENCHING INHIBITOR receive FDA 510(k) clearance?

MYOHEALTH CLENCHING INHIBITOR received FDA 510(k) clearance on 2004-08-27, under 510(k) number K040315.

Who is the listed applicant for MYOHEALTH CLENCHING INHIBITOR?

The FDA 510(k) record lists Mci-Myohealth Systems as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MYOHEALTH CLENCHING INHIBITOR?

The FDA product code for MYOHEALTH CLENCHING INHIBITOR is MQC.

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: MQC)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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