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FDA 510(k)

MY BREAST FRIEND, BREAST SELF-EXAM PAD

K-Number: K023390 · 2002-11-26

Decision Date2002-11-26
Product CodeIXH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MY BREAST FRIEND, BREAST SELF-EXAM PAD is the device name listed in this FDA 510(k) record. The listed applicant is Mbf Sales, LLC. It received FDA 510(k) clearance on 2002-11-26 under 510(k) number K023390. The device is classified under product code IXH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MY BREAST FRIEND, BREAST SELF-EXAM PAD?

MY BREAST FRIEND, BREAST SELF-EXAM PAD is a medical device that received FDA 510(k) clearance on 2002-11-26. The listed applicant is Mbf Sales, LLC. The 510(k) number is K023390.

When did MY BREAST FRIEND, BREAST SELF-EXAM PAD receive FDA 510(k) clearance?

MY BREAST FRIEND, BREAST SELF-EXAM PAD received FDA 510(k) clearance on 2002-11-26, under 510(k) number K023390.

Who is the listed applicant for MY BREAST FRIEND, BREAST SELF-EXAM PAD?

The FDA 510(k) record lists Mbf Sales, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MY BREAST FRIEND, BREAST SELF-EXAM PAD?

The FDA product code for MY BREAST FRIEND, BREAST SELF-EXAM PAD is IXH.

Related Clinical Trials

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.

Related Devices (Code: IXH)

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.

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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