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FDA 510(k)

LIV BREAST SELF EXAMINATION AID

K-Number: K070344 · 2007-03-08

ApplicantLiv International USA, Inc.
Decision Date2007-03-08
Product CodeIZH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

LIV BREAST SELF EXAMINATION AID is the device name listed in this FDA 510(k) record. The listed applicant is Liv International USA, Inc.. It received FDA 510(k) clearance on 2007-03-08 under 510(k) number K070344. The device is classified under product code IZH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIV BREAST SELF EXAMINATION AID?

LIV BREAST SELF EXAMINATION AID is a medical device that received FDA 510(k) clearance on 2007-03-08. The listed applicant is Liv International USA, Inc.. The 510(k) number is K070344.

When did LIV BREAST SELF EXAMINATION AID receive FDA 510(k) clearance?

LIV BREAST SELF EXAMINATION AID received FDA 510(k) clearance on 2007-03-08, under 510(k) number K070344.

Who is the listed applicant for LIV BREAST SELF EXAMINATION AID?

The FDA 510(k) record lists Liv International USA, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LIV BREAST SELF EXAMINATION AID?

The FDA product code for LIV BREAST SELF EXAMINATION AID is IZH.

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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.

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