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FDA 510(k)

DeepCatch

K-Number: K223556 · 2023-06-16

ApplicantMedical IP Co., Ltd.
Decision Date2023-06-16
Product CodeQIH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

DeepCatch is a medical device manufactured by Medical IP Co., Ltd.. It received FDA 510(k) clearance on 2023-06-16 under approval number K223556. The device is classified under product code QIH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DeepCatch?

DeepCatch is a medical device that received FDA 510(k) clearance on 2023-06-16. It is manufactured by Medical IP Co., Ltd.. The 510(k) number is K223556.

When was DeepCatch approved by the FDA?

DeepCatch received FDA 510(k) clearance on 2023-06-16, under approval number K223556.

What company makes DeepCatch?

DeepCatch is manufactured by Medical IP Co., Ltd..

What is the FDA product code for DeepCatch?

The FDA product code for DeepCatch is QIH.

Other Devices by Medical IP Co., Ltd.

K191026MEDIP PRO

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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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