K221860
- 510(k) number
- K221860
- Device name
- PLPT LDV(Low Dead Volume) LC(Luer-Cone) Sterile Syringe, PLPT LDV(Low Dead Volume) LL(Luer-Lock) Sterile Syringe
- Applicant
- Poonglim Pharmatech, Inc. KR
- Product code
- QNQ — Low Dead Space Piston Syringe
- Decision date
- 2023-09-15
- Date received
- 2022-06-27
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General Hospital
PDFDownload 510(k) SummaryArchived here · 0.6 MB · U.S. public domain
Also available from FDA: K221860.pdf
Official FDA record: K221860
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.