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

ANEROID SPHYGMOMANOMETER WITH STETHOSCOPE, MODEL LD-100

K Number: K092245 · Decision Oct 28, 2009
Classifications
1
FEI Numbers
172
Registration Numbers
172
Same Product Code
197
Applicant Total
12
Review Days
92

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Basic Information

Device Name
ANEROID SPHYGMOMANOMETER WITH STETHOSCOPE, MODEL LD-100
K Number
K092245
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1120
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Honsun (Nantong) Co., Ltd.
Date Received
July 28, 2009
Decision Date
October 28, 2009
Product Code
DXQ
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
DXQ Blood Pressure Cuff

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Other Clearances by Honsun (Nantong) Co., Ltd.

K Number Device Name
K252399 Portable Oxygen Concentrator
K260260 Automatic Digital Blood Pressure Monitor (LD-587, LD-528, LD-562, LD-581, LD-521, LD-527, LD-572 & LD-569)
K251795 Wrist automatic blood pressure monitor (LD-735, LD-752, LD-753)
K211629 Infrared forehead thermometer LD-FT-100B
K192500 Aneroid sphygmomanometer with stethoscope, Aneroid sphygmomanometer
K170866 Scian Automatic Digital Blood Pressure Monitor, Model: LD-576, LD-575 & LD-579
K170466 Automatic Blood Pressure Monitor Model LD-518 & LD-537
K170454 Automatic Blood Pressure Monitor Model LD-562U, LD-588U & LD-533U
K132627 AUTOMATIC DIGITAL BLOOD PRESSURE MONITOR
K130925 AUTOMATIC BLOOD PRESSURE MONITOR
Search all 12 clearances from Honsun (Nantong) Co., Ltd. →