FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇳 China

NEUCOLONCARE

K Number: K110077 · Decision Jan 28, 2011
Classifications
1
FEI Numbers
609
Registration Numbers
609
Same Product Code
2221
Applicant Total
20
Review Days
17

Basic Information

Device Name
NEUCOLONCARE
K Number
K110077
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.2050
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
NEUSOFT MEDICAL SYSTEMS CO., LTD.
Date Received
January 11, 2011
Decision Date
January 28, 2011
Product Code
LLZ
Advisory Committee
Radiology
Review Advisory Committee
RA
Third Party
Y

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 NEUSOFT MEDICAL SYSTEMS CO., LTD.

K Number Device Name
K151383 NeuViz 128 Multi-slice CT Scanner System
K151403 Positron Emission Tomography (PET) and Computed Tomography (CT) System, Positron Emission Tomography (PET) and Computed Tomography (CT) System
K133373 CLEARVIEW
K121792 NEUVIZ 64 MULTI-SLICE CT SCANNER SYSTEM
K102435 BEYONDIMAGE WORKSTATION
K092742 NEUVIZ 16 MULTI-SLICE CT SCANNER SYSTEM
K092237 NSM-S15 SYSTEM
K092235 BEYONDIMAGE WORKSTATION
K090552 UROCARE
K090173 NEUVIZ 16 MULTI-SLICE CT SCANNER SYSTEM
Search all 20 clearances from NEUSOFT MEDICAL SYSTEMS CO., LTD. →