iMedium Single Step; iMedium Single Step with HSA; iMedium Single Step with rHA— 510(k) K193522
Substantially EquivalentKitazato Corporation
FDA 510(k) clearance K193522 for iMedium Single Step; iMedium Single Step with HSA; iMedium Single Step with rHA, Substantially Equivalent on 2020-08-25. Applicant: Kitazato Corporation.
Clearance details
- Applicant
- Kitazato Corporation
- Product code
- Code MQL
- Advisory panel
- Obstetrics/Gynecology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Fuji-Shi, JP
Data sourced from openFDA. This site is unofficial and independent of the FDA.