Cumulus Remover— 510(k) K182002
Substantially EquivalentKitazato Corporation
FDA 510(k) clearance K182002 for Cumulus Remover, Substantially Equivalent on 2018-10-23. Applicant: Kitazato Corporation. Device class: 2.
Clearance details
- Applicant
- Kitazato Corporation
- Product code
- Code MQL
- Device class
- Class 2
- Regulation
- 21 CFR 884.6180
- Advisory panel
- Obstetrics/Gynecology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Shizuoka, JP
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Data sourced from openFDA. This site is unofficial and independent of the FDA.