FDA 510(k)
FDA class 2
Substantially Equivalent
🇩🇪 Germany
Vigilant Software Suite Vigilant Master Med
K Number: K210075
·
Decision Mar 1, 2022
Classifications
1
FEI Numbers
26
Registration Numbers
26
Same Product Code
9
Applicant Total
12
Review Days
413
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Basic Information
- Device Name
- Vigilant Software Suite Vigilant Master Med
- K Number
- K210075
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 880.5725
- Medical Specialty
- General Hospital
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Fresenius Kabi AG
- Date Received
- January 12, 2021
- Decision Date
- March 1, 2022
- Product Code
- PHC
- Advisory Committee
- General Hospital
- Review Advisory Committee
- HO
- Third Party
- N
Classifications
This FDA 510(k) entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| PHC | Infusion Safety Management Software | FDA class 2 | General Hospital |
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|---|---|---|---|
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| K160735 | CATSmart | Sep 16, 2016 | Substantially Equivalent |