K252512
- 510(k) number
- K252512
- Device name
- Armada 14 NC PTA Catheter
- Applicant
- ABBOTT MEDICAL CA · US
- Product code
- LIT — Catheter, Angioplasty, Peripheral, Transluminal
- Decision date
- 2026-02-13
- Date received
- 2025-08-11
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Cardiovascular
PDFDownload 510(k) SummaryArchived here · 2.6 MB · U.S. public domain
Also available from FDA: K252512.pdf
Official FDA record: K252512
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.