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

BLOOD PRESSURE METER, MODEL CH-432

K Number: K052046 · Decision Oct 19, 2005
Classifications
1
FEI Numbers
428
Registration Numbers
428
Same Product Code
1216
Applicant Total
8
Review Days
82

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
BLOOD PRESSURE METER, MODEL CH-432
K Number
K052046
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
870.1130
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Citizen Watch Co., Ltd.
Date Received
July 29, 2005
Decision Date
October 19, 2005
Product Code
DXN
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
Y

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 Citizen Watch Co., Ltd.

K Number Device Name
K061161 BLOOD PRESSURE METER, MODEL CH-311B
K001244 BLOOD PRESSURE METER, MODELS CH-631B, CH-631D, CH-632B, CH-632D
K984223 BLOOD PRESSURE METER, MODELS CH-491, CH-481, CH-471
K973061 CH-601A AND CH-601B DIGITAL WRIST SPHYGMOMANOMETER (CH-601A/CH-601B)
K954547 CH-502A & CH520B DIGITAL FINGER SPHYGMOMANOMETER
K923344 ELECTRONIC DIGITAL BLOOD PRESSURE MONITOR
K911965 ELECTRONIC DIGITAL BLOOD PRESSURE/PULSE MONITOR