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 | Device Class | Medical Specialty |
|---|---|---|---|
| DSI | Detector And Alarm, Arrhythmia | FDA class 2 | Cardiovascular |
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Other Clearances by Ppg Industries, Inc.
| K Number | Device Name | ||
|---|---|---|---|
| K922631 | STATPAL II BLOOD GAS ANALYSIS SYSTEM | Nov 10, 1992 | Substantially Equivalent |
| K913358 | MIDAS SYSTEM(TM) 5100 PHYSIOLOG MONIT/RECORD SYST | Dec 20, 1991 | Substantially Equivalent |
| K914560 | STAT PAL SENSYR SYRINGE ASSEMBLY FOR USE W/STATPAL | Nov 29, 1991 | Substantially Equivalent |
| K912627 | MIDAS SYSTEM 2500, PHYSIOLOGICAL MONITORING SYSTEM | Sep 10, 1991 | Substantially Equivalent |
| K903965 | STATPAL BLOOD GAS MONITORING SYSTEM | Dec 26, 1990 | Substantially Equivalent |
| K901514 | XR MODEL H PHYSIOLOGICAL MONITOR & RECORDING SYS. | Nov 16, 1990 | Substantially Equivalent |
| K901132 | SARA SATCAP | May 22, 1990 | Substantially Equivalent |
| K896442 | PPG BIOMEDICAL VENTILATOR MODEL IRISA | Apr 16, 1990 | Substantially Equivalent |
| K900700 | SMU 611 UNIVERSALMONITOR | Apr 3, 1990 | Substantially Equivalent |
| K890875 | CARDIOTEST EK53/EK53R, CARDIOGNOST EK56/EK512 | Oct 17, 1989 | Substantially Equivalent |