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

ArcCHECK-MR

K Number: K160057 · Decision May 13, 2016
Classifications
1
FEI Numbers
114
Registration Numbers
114
Same Product Code
733
Applicant Total
11
Review Days
122

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
ArcCHECK-MR
K Number
K160057
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.5050
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Sun Nuclear Corporation
Date Received
January 12, 2016
Decision Date
May 13, 2016
Product Code
IYE
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
IYE Accelerator, Linear, Medical

Similar 510(k) Clearances

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

View all

Other Clearances by Sun Nuclear Corporation

K Number Device Name
K170307 SunCHECK
K161946 DoseCHECK
K142617 ArcCHECK
K150848 Dose Calculator
K142142 QUALITY REPORTS
K142431 WaterProof PROFILER
K141800 PERFRACTION
K131862 3DVH
K131466 MAPCHECK2, ARCCHECK
K131704 EPIDOSE
Search all 11 clearances from Sun Nuclear Corporation →