MENTOR MEMORYSHAPE RESTERILIZABLE GEL SIZER— 510(k) K131853
Substantially EquivalentMentor Worldwide, LLC
FDA 510(k) clearance K131853 for MENTOR MEMORYSHAPE RESTERILIZABLE GEL SIZER, Substantially Equivalent on 2013-07-17. Applicant: Mentor Worldwide, LLC.
Clearance details
- Applicant
- Mentor Worldwide, LLC
- Product code
- Code MRD
- Advisory panel
- Unknown
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Location
- Santa Barbara, CA, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.