INTUTIVE SURGICAL DA VINCI SINGLE SITE INSTRUMENTS AND ACCESSORIES— 510(k) K112208

Unknown

Intuitive Surgical, Inc.

FDA 510(k) clearance K112208 for INTUTIVE SURGICAL DA VINCI SINGLE SITE INSTRUMENTS AND ACCESSORIES, Unknown on 2011-12-08. Applicant: Intuitive Surgical, Inc..

Clearance details

Applicant: Intuitive Surgical, Inc.
Product code: Code NAY
Advisory panel: Gastroenterology, Urology
Date received: 2011-08-01
Decision date: 2011-12-08
Decision: Unknown
Clearance type: Traditional
Location: Sunnyvale, CA, US

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Adverse events under product code NAY

product code NAY

Death: 433
Injury: 7,927
Malfunction: 93,790
Other: 19
Total: 102,169

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.