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FDA 510(k)

OMNIVISION

K-Number: K110040 · 2011-01-26

ApplicantModern Module, Inc.
Decision Date2011-01-26
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

OMNIVISION is the device name listed in this FDA 510(k) record. The listed applicant is Modern Module, Inc.. It received FDA 510(k) clearance on 2011-01-26 under 510(k) number K110040. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OMNIVISION?

OMNIVISION is a medical device that received FDA 510(k) clearance on 2011-01-26. The listed applicant is Modern Module, Inc.. The 510(k) number is K110040.

When did OMNIVISION receive FDA 510(k) clearance?

OMNIVISION received FDA 510(k) clearance on 2011-01-26, under 510(k) number K110040.

Who is the listed applicant for OMNIVISION?

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

What is the FDA product code for OMNIVISION?

The FDA product code for OMNIVISION is LLZ.

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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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