Vivatmo pro— 510(k) K233775
Substantially EquivalentBosch Healthcare Solutions GmbH
FDA 510(k) clearance K233775 for Vivatmo pro, Substantially Equivalent on 2024-02-22. Applicant: Bosch Healthcare Solutions GmbH. Device class: 2.
Clearance details
- Applicant
- Bosch Healthcare Solutions GmbH
- Product code
- Code MXA
- Device class
- Class 2
- Regulation
- 21 CFR 862.3080
- Advisory panel
- Clinical Toxicology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Waiblingen, DE
Recent devices under product code MXA
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