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

Q4500 STREE TEST MONITOR

K Number: K910017 · Decision Nov 5, 1991
Classifications
1
FEI Numbers
184
Registration Numbers
184
Same Product Code
570
Applicant Total
164
Review Days
306

Basic Information

Device Name
Q4500 STREE TEST MONITOR
K Number
K910017
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2340
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
QUINTON, INC.
Date Received
January 3, 1991
Decision Date
November 5, 1991
Product Code
DPS
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
DPS Electrocardiograph

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