K233268
- 510(k) number
- K233268
- Device name
- Impress Angiographic Catheter
- Applicant
- Merit Medical Systems, Inc. UT · US
- Product code
- DQO — Catheter, Intravascular, Diagnostic
- Decision date
- 2024-05-22
- Date received
- 2023-09-29
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Cardiovascular
PDFDownload 510(k) SummaryArchived here · 2.7 MB · U.S. public domain
Also available from FDA: K233268.pdf
Official FDA record: K233268
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.