510(k) K131853
K131853 is an FDA 510(k) premarket notification submitted by Mentor Worldwide, LLC for the device "MENTOR MEMORYSHAPE RESTERILIZABLE GEL SIZER". The FDA issued a decision of Substantially Equivalent on July 17, 2013. The device falls under product code MRD (Mammary Sizer), a Class U device. Mentor Worldwide, LLC has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- July 17, 2013
- Date Received
- June 21, 2013
- Clearance Type
- Special
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Mammary Sizer
- Device Class
- Class U
- Regulation Number
- Review Panel
- SU
- Submission Type