Meridian Vaginal Positioning System (VPS)— 510(k) K173501
Substantially EquivalentColoplast
FDA 510(k) clearance K173501 for Meridian Vaginal Positioning System (VPS), Substantially Equivalent on 2018-02-09. Applicant: Coloplast. Device class: 2.
Clearance details
- Applicant
- Coloplast
- Product code
- Code PWK
- Device class
- Class 2
- Regulation
- 21 CFR 884.4910
- Advisory panel
- Obstetrics/Gynecology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Plymouth, MN, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.