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

VersaOne Bladeless Trocar

K Number: K162584 · Decision Oct 18, 2016
Classifications
1
FEI Numbers
573
Registration Numbers
573
Same Product Code
1391
Applicant Total
80
Review Days
32

Basic Information

Device Name
VersaOne Bladeless Trocar
K Number
K162584
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
876.1500
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
COVIDIEN
Date Received
September 16, 2016
Decision Date
October 18, 2016
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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