FDA 510(k) clearance · back to tracker
da Vinci Surgical System (IS5000)
Intuitive Surgical, Inc. cleared K243641 on 2024-12-16, decision: substantially equivalent
K-number
K243641
Sponsor
Intuitive Surgical, Inc.
Device
da Vinci Surgical System (IS5000)
Class
Class II
Decision
Substantially Equivalent
Decision date
2024-12-16
Product code
NAY
Advisory committee
Gastroenterology, Urology
Medical specialty
Gastroenterology, Urology
Regulation number
876.1500
Official FDA record
Open K243641on 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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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.