VersaPump Infusion System— 510(k) K230883
Substantially EquivalentEmed Technologies Corporation
FDA 510(k) clearance K230883 for VersaPump Infusion System, Substantially Equivalent on 2023-11-28. Applicant: Emed Technologies Corporation.
Clearance details
- Applicant
- Emed Technologies Corporation
- Product code
- Code PKP
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- El Dorado Hills, CA, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.