K251375
- 510(k) number
- K251375
- Device name
- PuraCath Firefly Needleless Connector IT (9005)
- Applicant
- Puracath Medical, Inc. CA · US
- Product code
- FPA — Set, Administration, Intravascular
- Decision date
- 2026-02-12
- Date received
- 2025-05-02
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General Hospital
PDFDownload 510(k) SummaryArchived here · 0.5 MB · U.S. public domain
Also available from FDA: K251375.pdf
Official FDA record: K251375
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.