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FDA 510(k)

CORVIEW

K-Number: K131158 · 2013-08-21

ApplicantMarrek, Inc.
Decision Date2013-08-21
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CORVIEW is the device name listed in this FDA 510(k) record. The listed applicant is Marrek, Inc.. It received FDA 510(k) clearance on 2013-08-21 under 510(k) number K131158. 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 CORVIEW?

CORVIEW is a medical device that received FDA 510(k) clearance on 2013-08-21. The listed applicant is Marrek, Inc.. The 510(k) number is K131158.

When did CORVIEW receive FDA 510(k) clearance?

CORVIEW received FDA 510(k) clearance on 2013-08-21, under 510(k) number K131158.

Who is the listed applicant for CORVIEW?

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

What is the FDA product code for CORVIEW?

The FDA product code for CORVIEW is LLZ.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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