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

IRIS 1.0 System

K Number: K182643 · Decision Feb 22, 2019
Classifications
1
FEI Numbers
609
Registration Numbers
609
Same Product Code
2221
Applicant Total
12
Review Days
151

Basic Information

Device Name
IRIS 1.0 System
K Number
K182643
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.2050
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Intuitive Surgical
Date Received
September 24, 2018
Decision Date
February 22, 2019
Product Code
LLZ
Advisory Committee
Radiology
Review Advisory Committee
RA
Third Party
N

Classifications

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

Product Code Device Name
LLZ System, Image Processing, Radiological

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