K231707
- 510(k) number
- K231707
- Device name
- ResQ Administration Set
- Applicant
- Q For Plastic Industries EG
- Product code
- FPA — Set, Administration, Intravascular
- Decision date
- 2024-01-03
- Date received
- 2023-06-12
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Flag
- Third-party review
- Advisory committee
- General Hospital
PDFDownload 510(k) SummaryArchived here · 2.6 MB · U.S. public domain
Also available from FDA: K231707.pdf
Official FDA record: K231707
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.