Vigilant Software Suite Vigilant Master Med— 510(k) K210075
Substantially EquivalentFresenius Kabi AG
FDA 510(k) clearance K210075 for Vigilant Software Suite Vigilant Master Med, Substantially Equivalent on 2022-03-01. Applicant: Fresenius Kabi AG. Device class: 2.
Clearance details
- Applicant
- Fresenius Kabi AG
- Product code
- Code PHC
- Device class
- Class 2
- Regulation
- 21 CFR 880.5725
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Bad Homburg, DE
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Data sourced from openFDA. This site is unofficial and independent of the FDA.