GelPOINT V-Path Vaginal Access System— 510(k) K220969
Substantially EquivalentApplied Medical Resources Corporation
FDA 510(k) clearance K220969 for GelPOINT V-Path Vaginal Access System, Substantially Equivalent on 2022-09-16. Applicant: Applied Medical Resources Corporation. Device class: 2.
Clearance details
- Applicant
- Applied Medical Resources Corporation
- Product code
- Code MOK
- Device class
- Class 2
- Regulation
- 21 CFR 884.1630
- Advisory panel
- Obstetrics/Gynecology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Rancho Santa, CA, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.