Nest VT Vitrification Device— 510(k) K233177
Substantially EquivalentCook Incorporated
FDA 510(k) clearance K233177 for Nest VT Vitrification Device, Substantially Equivalent on 2024-03-08. Applicant: Cook Incorporated. Device class: 2.
Clearance details
- Applicant
- Cook Incorporated
- Product code
- Product code MQK
- Device class
- Class 2
- Regulation
- 21 CFR 884.6160
- Advisory panel
- Obstetrics/Gynecology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Bloomington, IN, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.