FDA 510(k) clearance · back to tracker
Liberant RX Aspiration Catheter
Medtronic Interventional Vascular, Inc. cleared K253589 on 2026-04-23, decision: substantially equivalent
K-number
K253589
Sponsor
Medtronic Interventional Vascular, Inc.
Device
Liberant RX Aspiration Catheter
Class
Class II
Decision
Substantially Equivalent
Decision date
2026-04-23
Product code
QEZ
Advisory committee
Cardiovascular
Medical specialty
Cardiovascular
Regulation number
870.5150
Official FDA record
Open K253589on accessdata.fda.gov →
FDA's authoritative 510(k) summary page. Includes the decision letter, predicate references, and downloadable substantial-equivalence determination.
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Raw record →
Machine-readable JSON. Useful for cross-referencing classification, product code, and advisory committee fields.
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Public 510(k) database, U.S. Food and Drug Administration, accessed via openFDA. Page refreshed weekly.