K240624
- 510(k) number
- K240624
- Device name
- InfuLife
- Applicant
- First Medical Source, LLC CA · US
- Product code
- MEB — Pump, Infusion, Elastomeric
- Decision date
- 2024-11-05
- Date received
- 2024-03-05
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General Hospital
PDFDownload 510(k) SummaryArchived here · 2.7 MB · U.S. public domain
Also available from FDA: K240624.pdf
Official FDA record: K240624
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.