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

ELECTRONIC SPHYGMOMANOMETER

K Number: K110774 · Decision May 13, 2011
Classifications
1
FEI Numbers
428
Registration Numbers
428
Same Product Code
1216
Applicant Total
12
Review Days
53

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Basic Information

Device Name
ELECTRONIC SPHYGMOMANOMETER
K Number
K110774
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1130
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Contec Medical System Co., Ltd.
Date Received
March 21, 2011
Decision Date
May 13, 2011
Product Code
DXN
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

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

Product Code Device Name
DXN System, Measurement, Blood-Pressure, Non-Invasive

Similar 510(k) Clearances

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Other Clearances by Contec Medical System Co., Ltd.

K Number Device Name
K180837 CONTEC Oxygen Concentrator
K131900 CONTEC ELECTROCARDIOGRAPH
K101273 DYNAMIC ECG SYSTEM MODEL TLC5000
K110156 AMBULATORY BLLOD PRESSURE MONITOR, ELECTRONIC SPHYGMOMANOMETER,
K101692 PATIENT MONITOR
K101127 PATIENT MONITOR, MODEL PM50
K090936 SINGLE-CHANNEL HANDHELD ELECTROCARDIOGRAPH, MODEL ECG80A
K090671 PULSE OXIMETER, MODELS CMS50E, CMS50F, CMS60C, CMS60D
K082480 CONTEC POCKET FETAL DOPPLER
K082641 FINGERTIP PULSE OXIMETER, MODELS CMS-50D, CMS-50L, CMS-50DL
Search all 12 clearances from Contec Medical System Co., Ltd. →