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

DOME S10

K Number: K132770 · Decision Jan 30, 2014
Classifications
1
FEI Numbers
609
Registration Numbers
609
Same Product Code
2221
Applicant Total
6
Review Days
148

Basic Information

Device Name
DOME S10
K Number
K132770
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.2050
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
NDS SURGICAL IMAGING
Date Received
September 4, 2013
Decision Date
January 30, 2014
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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K080320 PRIMEVUE 21 3MP COLOR DISPLAY, MODEL AC-QX21-A9300