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FDA 510(k)

VITREAVIEW SOFTWARE 6.1

K-Number: K111892 · 2011-07-28

ApplicantVital Images, Inc.
Decision Date2011-07-28
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

VITREAVIEW SOFTWARE 6.1 is the device name listed in this FDA 510(k) record. The listed applicant is Vital Images, Inc.. It received FDA 510(k) clearance on 2011-07-28 under 510(k) number K111892. 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 VITREAVIEW SOFTWARE 6.1?

VITREAVIEW SOFTWARE 6.1 is a medical device that received FDA 510(k) clearance on 2011-07-28. The listed applicant is Vital Images, Inc.. The 510(k) number is K111892.

When did VITREAVIEW SOFTWARE 6.1 receive FDA 510(k) clearance?

VITREAVIEW SOFTWARE 6.1 received FDA 510(k) clearance on 2011-07-28, under 510(k) number K111892.

Who is the listed applicant for VITREAVIEW SOFTWARE 6.1?

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

What is the FDA product code for VITREAVIEW SOFTWARE 6.1?

The FDA product code for VITREAVIEW SOFTWARE 6.1 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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