K253262
- 510(k) number
- K253262
- Device name
- EmeryGlide (EG18008901)
- Applicant
- Nano4imaging GmbH DE
- Product code
- DQX — Wire, Guide, Catheter
- Decision date
- 2026-03-06
- Date received
- 2025-09-29
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Cardiovascular
PDFDownload 510(k) SummaryArchived here · 3.1 MB · U.S. public domain
Also available from FDA: K253262.pdf
Official FDA record: K253262
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.