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

SYNAPSE 3D COLON ANALYSIS

K Number: K123566 · Decision Jan 22, 2013
Classifications
1
FEI Numbers
609
Registration Numbers
609
Same Product Code
2221
Applicant Total
20
Review Days
63

Basic Information

Device Name
SYNAPSE 3D COLON ANALYSIS
K Number
K123566
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.2050
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
FUJIFILM MEDICAL SYSTEMS U.S.A., INC.
Date Received
November 20, 2012
Decision Date
January 22, 2013
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

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (LLZ), ordered by most recent decision date.

View all

Other Clearances by FUJIFILM MEDICAL SYSTEMS U.S.A., INC.

K Number Device Name
K152257 Fujifilm Duodenoscope Model ED-530XT
K162287 Synapse 3D Perfusion Analysis
K161186 Fujifilm Diathermic Slitter (FlushKnife), Fujifilm Diathermic Slitter (ClutchCutter)
K153464 FDR D-EVO flat Panel Detector System
K160108 Synapse PACS
K153483 Balloon controller PB-30
K143556 Fujifilm Double Balloon Endoscopes Models EN-530T and EN-580T
K151859 Synapse Cardiovascular
K141765 FDR D-EVO FLAT PANEL DETECTOR SYSTEM
K140149 EPX-4440HD DIGITAL VIDEO PROCESSOR
Search all 20 clearances from FUJIFILM MEDICAL SYSTEMS U.S.A., INC. →