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FDA 510(k)

MasteRad MX30

K-Number: K190601 · 2019-04-25

ApplicantMedicatech USA
Decision Date2019-04-25
Product CodeKPR
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MasteRad MX30 is a medical device manufactured by Medicatech USA. It received FDA 510(k) clearance on 2019-04-25 under approval number K190601. The device is classified under product code KPR. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MasteRad MX30?

MasteRad MX30 is a medical device that received FDA 510(k) clearance on 2019-04-25. It is manufactured by Medicatech USA. The 510(k) number is K190601.

When was MasteRad MX30 approved by the FDA?

MasteRad MX30 received FDA 510(k) clearance on 2019-04-25, under approval number K190601.

What company makes MasteRad MX30?

MasteRad MX30 is manufactured by Medicatech USA.

What is the FDA product code for MasteRad MX30?

The FDA product code for MasteRad MX30 is KPR.

Other Devices by Medicatech USA

K230918MasterX 800 Series

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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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