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

CARDIOTEST EK 53 R, CARDIOGNOST EK 56/ EK 512

K Number: K900246 · Decision Jul 3, 1990
Classifications
1
FEI Numbers
121
Registration Numbers
121
Same Product Code
397
Applicant Total
20
Review Days
167

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Basic Information

Device Name
CARDIOTEST EK 53 R, CARDIOGNOST EK 56/ EK 512
K Number
K900246
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1025
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Ppg Industries, Inc.
Date Received
January 17, 1990
Decision Date
July 3, 1990
Product Code
DSI
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
DSI Detector And Alarm, Arrhythmia

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Other Clearances by Ppg Industries, Inc.

K Number Device Name
K922631 STATPAL II BLOOD GAS ANALYSIS SYSTEM
K913358 MIDAS SYSTEM(TM) 5100 PHYSIOLOG MONIT/RECORD SYST
K914560 STAT PAL SENSYR SYRINGE ASSEMBLY FOR USE W/STATPAL
K912627 MIDAS SYSTEM 2500, PHYSIOLOGICAL MONITORING SYSTEM
K903965 STATPAL BLOOD GAS MONITORING SYSTEM
K901514 XR MODEL H PHYSIOLOGICAL MONITOR & RECORDING SYS.
K901132 SARA SATCAP
K896442 PPG BIOMEDICAL VENTILATOR MODEL IRISA
K900700 SMU 611 UNIVERSALMONITOR
K890875 CARDIOTEST EK53/EK53R, CARDIOGNOST EK56/EK512
Search all 20 clearances from Ppg Industries, Inc. →