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

DIGITAL BLOOD PRESSURE METER

K Number: K821437 · Decision May 28, 1982
Classifications
1
FEI Numbers
428
Registration Numbers
428
Same Product Code
1216
Applicant Total
5
Review Days
15

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
DIGITAL BLOOD PRESSURE METER
K Number
K821437
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1130
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Timex Medical Products Corp.
Date Received
May 13, 1982
Decision Date
May 28, 1982
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 Timex Medical Products Corp.

K Number Device Name
K841616 TIMEX HEALTHCHECK DIGITAL BP MONITOR
K841595 HEALTHCHECK HOME PREGNANCY TEST KIT
K840228 HEALTHCHECK AUTO INFLATE DIGITAL BP
K821436 ELECTRONIC DIGITAL THERMOMETER