MENTOR RESTERILIZABLE GEL BREAST IMPLANT SIZER— 510(k) K062421
Substantially EquivalentMentor Corporation
FDA 510(k) clearance K062421 for MENTOR RESTERILIZABLE GEL BREAST IMPLANT SIZER, Substantially Equivalent on 2006-10-10. Applicant: Mentor Corporation. Device class: Unclassified.
Clearance details
- Applicant
- Mentor Corporation
- Product code
- Code MRD
- Device class
- Unclassified
- Advisory panel
- Unknown
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Santa Barbara, CA, US
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More clearances from Mentor Corporation
view allRecalls naming K062421
K-number listed on FDA's recall recordMatched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K062421.
Data sourced from openFDA. This site is unofficial and independent of the FDA.