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FDA 510(k)

DR. HAYS BITE GUARD

K-Number: K014079 · 2002-02-22

ApplicantInventive Resources, Inc.
Decision Date2002-02-22
Product CodeMQC
DecisionSubstantially Equivalent

Device Summary

DR. HAYS BITE GUARD is the device name listed in this FDA 510(k) record. The listed applicant is Inventive Resources, Inc.. It received FDA 510(k) clearance on 2002-02-22 under 510(k) number K014079. The device is classified under product code MQC. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DR. HAYS BITE GUARD?

DR. HAYS BITE GUARD is a medical device that received FDA 510(k) clearance on 2002-02-22. The listed applicant is Inventive Resources, Inc.. The 510(k) number is K014079.

When did DR. HAYS BITE GUARD receive FDA 510(k) clearance?

DR. HAYS BITE GUARD received FDA 510(k) clearance on 2002-02-22, under 510(k) number K014079.

Who is the listed applicant for DR. HAYS BITE GUARD?

The FDA 510(k) record lists Inventive Resources, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DR. HAYS BITE GUARD?

The FDA product code for DR. HAYS BITE GUARD is MQC.

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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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