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FDA 510(k)

I Do

K-Number: K192294 · 2020-07-31

ApplicantI DO Biotech Co., Ltd.
Decision Date2020-07-31
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

I Do is a medical device manufactured by I DO Biotech Co., Ltd.. It received FDA 510(k) clearance on 2020-07-31 under approval number K192294. The device is classified under product code DZE. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the I Do?

I Do is a medical device that received FDA 510(k) clearance on 2020-07-31. It is manufactured by I DO Biotech Co., Ltd.. The 510(k) number is K192294.

When was I Do approved by the FDA?

I Do received FDA 510(k) clearance on 2020-07-31, under approval number K192294.

What company makes I Do?

I Do is manufactured by I DO Biotech Co., Ltd..

What is the FDA product code for I Do?

The FDA product code for I Do is DZE.

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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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