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FDA 510(k) Applications Submitted by INTUITIVE SURGICAL
FDA 510(k) Number
Submission Date
Device Name
Applicant
K191529
06/10/2019
da Vinci Xi Surgical System, da Vinci X Surgical System
Intuitive Surgical
K133845
12/18/2013
8MM TROCAR KIT
INTUITIVE SURGICAL
K133942
12/23/2013
ENDOSCOPE STERILIZATION TRAY
INTUITIVE SURGICAL
K182643
09/24/2018
IRIS 1.0 System
Intuitive Surgical
K152892
09/30/2015
da Vinci Xi Surgical System
INTUITIVE SURGICAL
K192803
09/30/2019
da Vinci Xi Surgical System, da Vinci X Surgical System
Intuitive Surgical
K141075
04/25/2014
SINGLE-SITE WRISTED NEEDLE DRIVER
INTUITIVE SURGICAL
K183224
11/20/2018
SureForm 45, SureForm 45 Reloads
Intuitive Surgical
K173721
12/05/2017
SureForm 60 and SureForm 60 Reloads
Intuitive Surgical
K182188
08/13/2018
Ion Endoluminal System ; Flexision Biopsy Needle
Intuitive Surgical
K231212
04/28/2023
da Vinci E-200 Electrosurgical Generator
Intuitive Surgical
K223039
09/29/2022
da Vinci E-200 Electrosurgical Generator
Intuitive Surgical
K191736
06/28/2019
da Vinci X/Xi 8mm Endoscope Plus, 0, da Vinci X/Xi 8mm Endoscope Plus, 30
Intuitive Surgical
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