FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

da Vinci X/Xi 8mm Endoscope Plus, 0, da Vinci X/Xi 8mm Endoscope Plus, 30

K Number: K191736 · Decision Jul 26, 2019
Classifications
1
FEI Numbers
71
Registration Numbers
71
Same Product Code
163
Applicant Total
17
Review Days
28

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Basic Information

Device Name
da Vinci X/Xi 8mm Endoscope Plus, 0, da Vinci X/Xi 8mm Endoscope Plus, 30
K Number
K191736
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
876.1500
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Intuitive Surgical
Date Received
June 28, 2019
Decision Date
July 26, 2019
Product Code
NAY
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
SU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
NAY System, Surgical, Computer Controlled Instrument

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K231212 da Vinci E-200 Electrosurgical Generator
K223039 da Vinci E-200 Electrosurgical Generator
K192803 da Vinci Xi Surgical System, da Vinci X Surgical System
K191529 da Vinci Xi Surgical System, da Vinci X Surgical System
K182643 IRIS 1.0 System
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