VagiVital Aktivgel
FDA 510(k) clearance K200098 · decided 2020-11-10
Clearance details
- K-number
- K200098
- Device name
- VagiVital Aktivgel
- Applicant
- Peptonic Medical AB
- Decision
- Substantially Equivalent
- Date received
- 2020-01-16
- Decision date
- 2020-11-10
- Days to decision
- 299 days
- Clearance type
- Traditional
- Product code
- NUC
- Device class
- 2
- Regulation number
- 884.5300
- Medical specialty
- Obstetrics/Gynecology
- Advisory committee
- Obstetrics/Gynecology
- Location
- Bromma, SE
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.