EEVA 2.0— 510(k) DEN120015
UnknownAuxogyn, Inc.
FDA 510(k) clearance DEN120015 for EEVA 2.0, Unknown on 2014-06-06. Applicant: Auxogyn, Inc.. Device class: 2.
Clearance details
- Applicant
- Auxogyn, Inc.
- Product code
- Code PBH
- Device class
- Class 2
- Regulation
- 21 CFR 884.6195
- Advisory panel
- Obstetrics/Gynecology
- Date received
- Decision date
- Decision
- Unknown
- Clearance type
- Post-NSE
- Location
- Hillsborough, CA, US
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