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

CARESTREAM VUE PACS

K Number: K122523 · Decision Oct 23, 2012
Classifications
1
FEI Numbers
609
Registration Numbers
609
Same Product Code
2221
Applicant Total
18
Review Days
64

Basic Information

Device Name
CARESTREAM VUE PACS
K Number
K122523
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.2050
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
CARESTREAM HEALTH, INC.
Date Received
August 20, 2012
Decision Date
October 23, 2012
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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Other Clearances by CARESTREAM HEALTH, INC.

K Number Device Name
K160723 OnSight 3D Extremity System
K153103 CARESTREAM Vue PACS
K152467 Touch Ultrasound
K153142 Carestream DRX-1 System with DRX Plus 4343 Detectors
K151774 CARESTREAM Vue Motion
K150342 Touch Ultrasound
K140271 TABLET VIEWER SOFTWARE FOR IMAGE SUITE
K133442 BONE SUPPRESSION SOFTWARE
K130567 DR LONG LENGTH IMAGING SOFTWARE
K120062 DRX-REVOLUTION MOBILE X-RAY SYSTEM
Search all 18 clearances from CARESTREAM HEALTH, INC. →