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

DT-100

K Number: K160358 · Decision Feb 24, 2017
Classifications
1
FEI Numbers
488
Registration Numbers
488
Same Product Code
797
Applicant Total
10
Review Days
381

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Basic Information

Device Name
DT-100
K Number
K160358
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.2910
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Mediana Co., Ltd.
Date Received
February 9, 2016
Decision Date
February 24, 2017
Product Code
FLL
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
FLL Continuous Measurement Thermometer

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K110630 F10
K100225 PULSE OXIMETER MODEL P10
K100217 LUCON M-SERIES PATIENT MONITOR, MODELS M20 AND M30
K051375 VITAL SIGNS MONITOR