MENTOR ALLOPLASTIC SPERMATOCELE— 510(k) K863565

Name: FDA 510(k) clearance K863565
Creator: U.S. Food and Drug Administration
Published: 1986-11-19

Substantially Equivalent

Mentor Corp.

FDA 510(k) clearance K863565 for MENTOR ALLOPLASTIC SPERMATOCELE, Substantially Equivalent on 1986-11-19. Applicant: Mentor Corp.. Device class: Unclassified.

Clearance details

Applicant: Mentor Corp.
Product code: Code LQS
Device class: Unclassified
Advisory panel: Unknown
Date received: 1986-09-12
Decision date: 1986-11-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Goleta, CA, US

Download summary PDF View on FDA.gov ↗

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