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FDA 510(k)

MYAH

K-Number: K222933 · 2023-06-29

ApplicantVisia Imaging S.R.L.
Decision Date2023-06-29
Product CodeMXK
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

MYAH is a medical device manufactured by Visia Imaging S.R.L.. It received FDA 510(k) clearance on 2023-06-29 under approval number K222933. The device is classified under product code MXK. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MYAH?

MYAH is a medical device that received FDA 510(k) clearance on 2023-06-29. It is manufactured by Visia Imaging S.R.L.. The 510(k) number is K222933.

When was MYAH approved by the FDA?

MYAH received FDA 510(k) clearance on 2023-06-29, under approval number K222933.

What company makes MYAH?

MYAH is manufactured by Visia Imaging S.R.L..

What is the FDA product code for MYAH?

The FDA product code for MYAH is MXK.

Related Clinical Trials

NCT06966349 Quantifying Ocular Surface Aberrations After Tear Film Interventions COMPLETED

Other Devices by Visia Imaging S.R.L.

K160327ALADDIN HW3.0 K211868MYAH

Related Devices (Code: MXK)

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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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