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

MICROLIFE UPPER ARM MANUAL BLOOD PRESSURE MONITOR, MODEL BP3MR1-H (BP A50)

K Number: K073397 · Decision Dec 20, 2007
Classifications
1
FEI Numbers
428
Registration Numbers
428
Same Product Code
1216
Applicant Total
13
Review Days
17

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Basic Information

Device Name
MICROLIFE UPPER ARM MANUAL BLOOD PRESSURE MONITOR, MODEL BP3MR1-H (BP A50)
K Number
K073397
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
870.1130
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Microlife Corp.
Date Received
December 3, 2007
Decision Date
December 20, 2007
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

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Other Clearances by Microlife Corp.

K Number Device Name
K122013 MICROLIFE UPPER ARM AUTOMATIC DIGITAL BLOOD PRESSURE MONITOR, CARDIO+ (BP4GAPO-2M)
K080337 MICROLIFE UPPER ARM AUTOMATIC DIGITAL BLOOD PRESSURE MONITOR, MODEL BP3MQ1-2D
K073398 MICROLIFE WRIST WATCH BLOOD PRESSURE MONITOR, MODEL BP3MK1-3 (BP W100)
K041411 MICROLIFE UPPER ARM BLOOD PRESSURE MONITOR, MODEL BP-3BTO-AP
K031024 MICROLIFE ELECTRONIC PEAK FLOW MONITOR, MODEL PF-100
K030961 MICROLIFE DIGITAL BASAL THERMOMETER, MODEL MT 1921
K021305 MICROLIFE WRIST WATCH BLOOD PRESSURE, MODEL BP-3BU1-5, WITH OPTIONAL THERMAL PRINTER
K020725 MICROLIFE DIGITAL INFRARED EAR THERMOMETER, MODEL IR1DE1
K013485 MICROLIFE UPPER ARM AUTOMATIC BLOOD PRESSURE MONITOR, MODEL BP-3BTO-1, WITH OPTIONAL THERMAL PRINTER, MODEL PR 1KA1
K003308 MICROLIFE DIGITAL INFRARED EAR THERMOMETER, IR1DAI, IR1DB1, IR1DD1
Search all 13 clearances from Microlife Corp. →