K241552
- 510(k) number
- K241552
- Device name
- MENTOR MemoryGel Enhance Single Use Gel Sizer
- Applicant
- Mentor Worldwide, LLC CA · US
- Product code
- MRD — Mammary Sizer
- Decision date
- 2024-09-06
- Date received
- 2024-05-31
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Unknown
PDFDownload 510(k) SummaryArchived here · 2.6 MB · U.S. public domain
Also available from FDA: K241552.pdf
Official FDA record: K241552
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.