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

FUKUDA DENSHI MODEL HJ-310

K Number: K901889 · Decision Jul 17, 1990
Classifications
1
FEI Numbers
420
Registration Numbers
420
Same Product Code
1186
Applicant Total
66
Review Days
82

Basic Information

Device Name
FUKUDA DENSHI MODEL HJ-310
K Number
K901889
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1130
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
FUKUDA DENSHI USA, INC.
Date Received
April 26, 1990
Decision Date
July 17, 1990
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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