FDA 510(k) FDA class 2 Substantially Equivalent 🇸🇪 Sweden

IPS CaseDesigner

K Number: K161634 · Decision Nov 10, 2016
Classifications
1
FEI Numbers
609
Registration Numbers
609
Same Product Code
2221
Applicant Total
60
Review Days
149

Basic Information

Device Name
IPS CaseDesigner
K Number
K161634
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.2050
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
NOBEL BIOCARE AB
Date Received
June 14, 2016
Decision Date
November 10, 2016
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 NOBEL BIOCARE AB

K Number Device Name
K161416 Multi-unit Abutment Plus
K161655 On1 Concept
K163122 NobelClinician, DTX Studio implant
K153534 NobelProcera HT ML Full Contour Zirconia Crown
K153036 NobelDesign Software
K160119 NobelSpeedy Groovy
K152836 TREFOIL System
K152093 NobelZygoma 45°
K142260 NobelActive
K133377 NOBELPROCERA ANGULATED SCREW CHANNEL ABUTMENT REPLACE
Search all 60 clearances from NOBEL BIOCARE AB →