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FDA 510(k)

miha bodytec II

K-Number: K201975 · 2021-03-11

ApplicantMiha Bodytec GmbH
Decision Date2021-03-11
Product CodeNGX
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

miha bodytec II is a medical device manufactured by Miha Bodytec GmbH. It received FDA 510(k) clearance on 2021-03-11 under approval number K201975. The device is classified under product code NGX. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the miha bodytec II?

miha bodytec II is a medical device that received FDA 510(k) clearance on 2021-03-11. It is manufactured by Miha Bodytec GmbH. The 510(k) number is K201975.

When was miha bodytec II approved by the FDA?

miha bodytec II received FDA 510(k) clearance on 2021-03-11, under approval number K201975.

What company makes miha bodytec II?

miha bodytec II is manufactured by Miha Bodytec GmbH.

What is the FDA product code for miha bodytec II?

The FDA product code for miha bodytec II is NGX.

Other Devices by Miha Bodytec GmbH

K182519Miha Bodytec II K221498Miha Bodytec II

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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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