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

AUTOMATED NON-INVASIVE BLOOD PRESSURE MONITOR, MODEL BPM-100

K Number: K994423 · Decision Mar 28, 2000
Classifications
1
FEI Numbers
428
Registration Numbers
428
Same Product Code
1216
Applicant Total
3
Review Days
90

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Basic Information

Device Name
AUTOMATED NON-INVASIVE BLOOD PRESSURE MONITOR, MODEL BPM-100
K Number
K994423
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1130
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Vsm Medtech , Ltd.
Date Received
December 29, 1999
Decision Date
March 28, 2000
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

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

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Other Clearances by Vsm Medtech , Ltd.

K Number Device Name
K023078 BPTRU VITAL SIGNS MONITOR, MODEL BPM-300, & BPTRU PORTABLE AUTOMATED NON-INVASIVE BLOOD PRESSURE AND TEMPERATURE MONITOR
K023055 BPTRU PORTABLE AUTOMATED NON-INVASIVE BLOOD PRESSURE MONITOR, MODEL BPM-200