MENTOR MEMORYSHAPE RESTERILIZABLE GEL SIZER— 510(k) K131853

Name: FDA 510(k) clearance K131853
Creator: U.S. Food and Drug Administration
Published: 2013-07-17

Substantially Equivalent

Mentor Worldwide, LLC

FDA 510(k) clearance K131853 for MENTOR MEMORYSHAPE RESTERILIZABLE GEL SIZER, Substantially Equivalent on 2013-07-17. Applicant: Mentor Worldwide, LLC. Device class: Unclassified.

Clearance details

Applicant: Mentor Worldwide, LLC
Product code: Code MRD
Device class: Unclassified
Advisory panel: Unknown
Date received: 2013-06-21
Decision date: 2013-07-17
Decision: Substantially Equivalent
Clearance type: Special
Location: Santa Barbara, CA, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.