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FDA 510(k)

MEDIP PRO

K-Number: K191026 · 2019-11-07

ApplicantMedical IP Co., Ltd.
Decision Date2019-11-07
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MEDIP PRO is a medical device manufactured by Medical IP Co., Ltd.. It received FDA 510(k) clearance on 2019-11-07 under approval number K191026. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDIP PRO?

MEDIP PRO is a medical device that received FDA 510(k) clearance on 2019-11-07. It is manufactured by Medical IP Co., Ltd.. The 510(k) number is K191026.

When was MEDIP PRO approved by the FDA?

MEDIP PRO received FDA 510(k) clearance on 2019-11-07, under approval number K191026.

What company makes MEDIP PRO?

MEDIP PRO is manufactured by Medical IP Co., Ltd..

What is the FDA product code for MEDIP PRO?

The FDA product code for MEDIP PRO is LLZ.

Other Devices by Medical IP Co., Ltd.

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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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