FDA 510(k) FDA class 2 Substantially Equivalent 🇹🇼 Taiwan

FULL AUTOMATIC (NIBP) BLOOD PRESSURE MONITOR

K Number: K130563 · Decision Jun 18, 2013
Classifications
1
FEI Numbers
428
Registration Numbers
428
Same Product Code
1216
Applicant Total
60
Review Days
106

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
FULL AUTOMATIC (NIBP) BLOOD PRESSURE MONITOR
K Number
K130563
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1130
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Health & Life Co., Ltd.
Date Received
March 4, 2013
Decision Date
June 18, 2013
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.

View all

Other Clearances by Health & Life Co., Ltd.

K Number Device Name
K211744 Non-Contact Infrared Thermometer, model HL710H
K211127 Full Automatic (NIBP) Blood Pressure Monitor, Model HL858DM
K200521 Full Automatic(NIBP) Blood Pressure Monitor
K190507 Full Automatic (NIBP) Blood Pressure Monitor
K190133 Full Automatic (NIBP) Blood Pressure Monitor-HL158UB
K190134 Full Automatic (NIBP) Blood Pressure Monitor-HL158TB
K180240 Full Automatic(NIBP) Blood Pressure Monitor
K162338 Full Automatic (NIBP) Blood Pressure Monitor
K160557 Full Automatic (NIBP) Blood Pressure Monitor
K161156 Full Automatic (NIBP) Blood Pressure Monitor
Search all 60 clearances from Health & Life Co., Ltd. →