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FDA 510(k)

MENTOR NIPPLE RECONSTRUCTION DEVICE

K-Number: K870059 · 1987-02-24

ApplicantMentor Corp.
Decision Date1987-02-24
Product Code
DecisionSubstantially Equivalent

Device Summary

MENTOR NIPPLE RECONSTRUCTION DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Mentor Corp.. It received FDA 510(k) clearance on 1987-02-24 under 510(k) number K870059. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MENTOR NIPPLE RECONSTRUCTION DEVICE?

MENTOR NIPPLE RECONSTRUCTION DEVICE is a medical device that received FDA 510(k) clearance on 1987-02-24. The listed applicant is Mentor Corp.. The 510(k) number is K870059.

When did MENTOR NIPPLE RECONSTRUCTION DEVICE receive FDA 510(k) clearance?

MENTOR NIPPLE RECONSTRUCTION DEVICE received FDA 510(k) clearance on 1987-02-24, under 510(k) number K870059.

Who is the listed applicant for MENTOR NIPPLE RECONSTRUCTION DEVICE?

The FDA 510(k) record lists Mentor Corp. as the applicant. This does not by itself establish the device manufacturer.

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Other records listing Mentor Corp. 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.

K130813MENTOR CPX 4 BREAST TISSUE EXPANDERS AND MENTOR CPX 4 WITH SUTURE TABS BREAST TISSUE EXPANDERSK053414MENTOR NOVASILK MESHK050008MENTOR SELF-CATH HYDROGEL INTERMITTENT CATHETERK042851MENTOR OBTAPE TRANS-OBTURATOR SURGICAL KITK040959MENTOR GENESIS PENILE PROSTHESISK031767MENTOR OBTAPE TRANS-OBTURATOR TAPE

View all 61 devices →

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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