FDA 510(k) FDA class 2 Substantially Equivalent 🇰🇷 South Korea

EzDent-i / E2 / Prora View

K Number: K161117 · Decision May 13, 2016
Classifications
1
FEI Numbers
609
Registration Numbers
609
Same Product Code
2221
Applicant Total
4
Review Days
23

Basic Information

Device Name
EzDent-i / E2 / Prora View
K Number
K161117
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
892.2050
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
EWOO SOFT CO., LTD.
Date Received
April 20, 2016
Decision Date
May 13, 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

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Other Clearances by EWOO SOFT CO., LTD.

K Number Device Name
K163533 EzDent-i; E2; ProraView
K161246 Ez3D-i / E3
K152746 Ez3D Plus