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

8MM TROCAR KIT

K Number: K133845 · Decision Feb 19, 2014
Classifications
1
FEI Numbers
548
Registration Numbers
548
Same Product Code
1422
Applicant Total
17
Review Days
63

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Basic Information

Device Name
8MM TROCAR KIT
K Number
K133845
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.1500
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Intuitive Surgical
Date Received
December 18, 2013
Decision Date
February 19, 2014
Product Code
GCJ
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
GCJ Laparoscope, General & Plastic Surgery

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K191529 da Vinci Xi Surgical System, da Vinci X Surgical System
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