FDA 510(k)

MEDIP PRO

K-Number: K191026 · 2019-11-07

Decision Date2019-11-07

Product CodeLLZ

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

MEDIP PRO is the device name listed in this FDA 510(k) record. The listed applicant is Medical IP Co., Ltd.. It received FDA 510(k) clearance on 2019-11-07 under 510(k) 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. The listed applicant is Medical IP Co., Ltd.. The 510(k) number is K191026.

When did MEDIP PRO receive FDA 510(k) clearance?

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

Who is the listed applicant for MEDIP PRO?

The FDA 510(k) record lists Medical IP Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MEDIP PRO?

The FDA product code for MEDIP PRO is LLZ.

Other records listing Medical IP Co., Ltd. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.