K251648
- 510(k) number
- K251648
- Device name
- GPS Advanced; GPS Advanced Cannula
- Applicant
- Prosidyan, Inc. NJ · US
- Product code
- FMF — Syringe, Piston
- Decision date
- 2025-06-24
- Date received
- 2025-05-29
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- General Hospital
PDFDownload 510(k) SummaryArchived here · 2.7 MB · U.S. public domain
Also available from FDA: K251648.pdf
Official FDA record: K251648
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.