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FDA 510(k)

MIDIVIEW SERIES OF MICROENDOSCOPES

K-Number: K051073 · 2006-05-17

ApplicantMillennium Devices, Inc.
Decision Date2006-05-17
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MIDIVIEW SERIES OF MICROENDOSCOPES is the device name listed in this FDA 510(k) record. The listed applicant is Millennium Devices, Inc.. It received FDA 510(k) clearance on 2006-05-17 under 510(k) number K051073. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MIDIVIEW SERIES OF MICROENDOSCOPES?

MIDIVIEW SERIES OF MICROENDOSCOPES is a medical device that received FDA 510(k) clearance on 2006-05-17. The listed applicant is Millennium Devices, Inc.. The 510(k) number is K051073.

When did MIDIVIEW SERIES OF MICROENDOSCOPES receive FDA 510(k) clearance?

MIDIVIEW SERIES OF MICROENDOSCOPES received FDA 510(k) clearance on 2006-05-17, under 510(k) number K051073.

Who is the listed applicant for MIDIVIEW SERIES OF MICROENDOSCOPES?

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

What is the FDA product code for MIDIVIEW SERIES OF MICROENDOSCOPES?

The FDA product code for MIDIVIEW SERIES OF MICROENDOSCOPES is GCJ.

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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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