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

Caremed patient cable and leadwires

K Number: K153188 · Decision Oct 24, 2016
Classifications
1
FEI Numbers
139
Registration Numbers
139
Same Product Code
104
Applicant Total
6
Review Days
356

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Basic Information

Device Name
Caremed patient cable and leadwires
K Number
K153188
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2900
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Shenzhen Caremed Medical Technology Co., Ltd.
Date Received
November 3, 2015
Decision Date
October 24, 2016
Product Code
DSA
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
DSA Cable, Transducer And Electrode, Patient, (Including Connector)

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (DSA), ordered by most recent decision date.

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Other Clearances by Shenzhen Caremed Medical Technology Co., Ltd.

K Number Device Name
K191279 Disposable SpO2 Sensor
K182751 Reusable Temperature Probe
K182755 Disposable Temperature Probe
K182433 Reusable Blood Pressure Cuff, Disposable Blood Pressure Cuff
K153184 Caremed Reusable & Disposable SPO2 Sensors