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FDA 510(k)

MICROSCOPE SYSTEM

K-Number: K041805 · 2004-09-21

ApplicantMiras Mirror Imaging Solutions, Ltd.
Decision Date2004-09-21
Product CodeEIA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

MICROSCOPE SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Miras Mirror Imaging Solutions, Ltd.. It received FDA 510(k) clearance on 2004-09-21 under 510(k) number K041805. The device is classified under product code EIA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MICROSCOPE SYSTEM?

MICROSCOPE SYSTEM is a medical device that received FDA 510(k) clearance on 2004-09-21. The listed applicant is Miras Mirror Imaging Solutions, Ltd.. The 510(k) number is K041805.

When did MICROSCOPE SYSTEM receive FDA 510(k) clearance?

MICROSCOPE SYSTEM received FDA 510(k) clearance on 2004-09-21, under 510(k) number K041805.

Who is the listed applicant for MICROSCOPE SYSTEM?

The FDA 510(k) record lists Miras Mirror Imaging Solutions, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MICROSCOPE SYSTEM?

The FDA product code for MICROSCOPE SYSTEM is EIA.

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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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