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FDA 510(k)

MITRA-LIFT

K-Number: K103812 · 2011-05-18

ApplicantSciencity Co., Ltd.
Decision Date2011-05-18
Product CodeKRH
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MITRA-LIFT is the device name listed in this FDA 510(k) record. The listed applicant is Sciencity Co., Ltd.. It received FDA 510(k) clearance on 2011-05-18 under 510(k) number K103812. The device is classified under product code KRH. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MITRA-LIFT?

MITRA-LIFT is a medical device that received FDA 510(k) clearance on 2011-05-18. The listed applicant is Sciencity Co., Ltd.. The 510(k) number is K103812.

When did MITRA-LIFT receive FDA 510(k) clearance?

MITRA-LIFT received FDA 510(k) clearance on 2011-05-18, under 510(k) number K103812.

Who is the listed applicant for MITRA-LIFT?

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

What is the FDA product code for MITRA-LIFT?

The FDA product code for MITRA-LIFT is KRH.

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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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