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FDA 510(k)

MYVISIONTRACK(TM)

K-Number: K121738 · 2013-02-22

ApplicantVital Art and Science Incorporated
Decision Date2013-02-22
Product CodeHOQ
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

MYVISIONTRACK(TM) is the device name listed in this FDA 510(k) record. The listed applicant is Vital Art and Science Incorporated. It received FDA 510(k) clearance on 2013-02-22 under 510(k) number K121738. The device is classified under product code HOQ. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MYVISIONTRACK(TM)?

MYVISIONTRACK(TM) is a medical device that received FDA 510(k) clearance on 2013-02-22. The listed applicant is Vital Art and Science Incorporated. The 510(k) number is K121738.

When did MYVISIONTRACK(TM) receive FDA 510(k) clearance?

MYVISIONTRACK(TM) received FDA 510(k) clearance on 2013-02-22, under 510(k) number K121738.

Who is the listed applicant for MYVISIONTRACK(TM)?

The FDA 510(k) record lists Vital Art and Science Incorporated as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MYVISIONTRACK(TM)?

The FDA product code for MYVISIONTRACK(TM) is HOQ.

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Related Devices (Code: HOQ)

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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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