da Vinci S/Si Endoscopes, da Vinci Xi Endoscopes
K-Number: K170641 · 2017-09-21
ApplicantIntuitive Surgical, Inc.
Decision Date2017-09-21
Product CodeNAY
Advisory CommitteeGU
DecisionSubstantially Equivalent
Device Summary
da Vinci S/Si Endoscopes, da Vinci Xi Endoscopes is a medical device manufactured by Intuitive Surgical, Inc.. It received FDA 510(k) clearance on 2017-09-21 under approval number K170641. The device is classified under product code NAY. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the da Vinci S/Si Endoscopes, da Vinci Xi Endoscopes?
da Vinci S/Si Endoscopes, da Vinci Xi Endoscopes is a medical device that received FDA 510(k) clearance on 2017-09-21. It is manufactured by Intuitive Surgical, Inc.. The 510(k) number is K170641.
When was da Vinci S/Si Endoscopes, da Vinci Xi Endoscopes approved by the FDA?
da Vinci S/Si Endoscopes, da Vinci Xi Endoscopes received FDA 510(k) clearance on 2017-09-21, under approval number K170641.
What company makes da Vinci S/Si Endoscopes, da Vinci Xi Endoscopes?
da Vinci S/Si Endoscopes, da Vinci Xi Endoscopes is manufactured by Intuitive Surgical, Inc..
What is the FDA product code for da Vinci S/Si Endoscopes, da Vinci Xi Endoscopes?
The FDA product code for da Vinci S/Si Endoscopes, da Vinci Xi Endoscopes is NAY.
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Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.