FDA 510(k) clearance · back to tracker
SmartClip Delivery Catheter (ADR-1715)
Elucent Medical cleared K260565 on 2026-05-14, decision: substantially equivalent
K-number
K260565
Sponsor
Elucent Medical
Device
SmartClip Delivery Catheter (ADR-1715)
Class
Class II
Decision
Substantially Equivalent
Decision date
2026-05-14
Product code
EOQ
Advisory committee
Ear, Nose, Throat
Medical specialty
Ear, Nose, Throat
Regulation number
874.4680
Official FDA record
Open K260565on accessdata.fda.gov →
FDA's authoritative 510(k) summary page. Includes the decision letter, predicate references, and downloadable substantial-equivalence determination.
openFDA JSON
Raw record →
Machine-readable JSON. Useful for cross-referencing classification, product code, and advisory committee fields.
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Drop K260565 into Compass and start a substantial-equivalence draft.
Compass pulls the predicate's intended use, technological characteristics, and performance data, maps them against your device, and produces a draft SE table aligned to FDA's 510(k) program guidance.
Try the sandboxSource
Public 510(k) database, U.S. Food and Drug Administration, accessed via openFDA. Page refreshed weekly.