K241426
- 510(k) number
- K241426
- Device name
- GPS Advanced; 5 cc GPS Advanced Cannula
- Applicant
- Prosidyan, Inc. NJ · US
- Product code
- FMF — Syringe, Piston
- Decision date
- 2024-07-10
- Date received
- 2024-05-20
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General Hospital
PDFDownload 510(k) SummaryArchived here · 0.9 MB · U.S. public domain
Also available from FDA: K241426.pdf
Official FDA record: K241426
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.