MENTOR NIPPLE RECONSTRUCTION DEVICE— 510(k) K870059

Substantially Equivalent

Mentor Corp.

FDA 510(k) clearance K870059 for MENTOR NIPPLE RECONSTRUCTION DEVICE, Substantially Equivalent on 1987-02-24. Applicant: Mentor Corp..

Clearance details

Applicant: Mentor Corp.
Advisory panel: Unknown
Date received: 1987-01-07
Decision date: 1987-02-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Goleta, CA, US

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