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FDA 510(k)

MITEK MICRO QUICKANCHOR

K-Number: K032078 · 2003-08-25

Decision Date2003-08-25
Product CodeNOV
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

MITEK MICRO QUICKANCHOR is the device name listed in this FDA 510(k) record. The listed applicant is Mitek Worldwide. It received FDA 510(k) clearance on 2003-08-25 under 510(k) number K032078. The device is classified under product code NOV. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MITEK MICRO QUICKANCHOR?

MITEK MICRO QUICKANCHOR is a medical device that received FDA 510(k) clearance on 2003-08-25. The listed applicant is Mitek Worldwide. The 510(k) number is K032078.

When did MITEK MICRO QUICKANCHOR receive FDA 510(k) clearance?

MITEK MICRO QUICKANCHOR received FDA 510(k) clearance on 2003-08-25, under 510(k) number K032078.

Who is the listed applicant for MITEK MICRO QUICKANCHOR?

The FDA 510(k) record lists Mitek Worldwide as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MITEK MICRO QUICKANCHOR?

The FDA product code for MITEK MICRO QUICKANCHOR is NOV.

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.

Other records listing Mitek Worldwide as applicant

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.

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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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