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FDA 510(k)

MEGVISION, MODEL EQ1000C SERIES

K-Number: K040051 · 2004-03-24

ApplicantEagle Technology, Inc.
Decision Date2004-03-24
Product CodeOLX
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

MEGVISION, MODEL EQ1000C SERIES is the device name listed in this FDA 510(k) record. The listed applicant is Eagle Technology, Inc.. It received FDA 510(k) clearance on 2004-03-24 under 510(k) number K040051. The device is classified under product code OLX. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEGVISION, MODEL EQ1000C SERIES?

MEGVISION, MODEL EQ1000C SERIES is a medical device that received FDA 510(k) clearance on 2004-03-24. The listed applicant is Eagle Technology, Inc.. The 510(k) number is K040051.

When did MEGVISION, MODEL EQ1000C SERIES receive FDA 510(k) clearance?

MEGVISION, MODEL EQ1000C SERIES received FDA 510(k) clearance on 2004-03-24, under 510(k) number K040051.

Who is the listed applicant for MEGVISION, MODEL EQ1000C SERIES?

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

What is the FDA product code for MEGVISION, MODEL EQ1000C SERIES?

The FDA product code for MEGVISION, MODEL EQ1000C SERIES is OLX.

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Related Devices (Code: OLX)

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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