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

CARDIAC OUTPUR/SATURATED VENOUS OXYGEN MODULE

K Number: K893867 · Decision Sep 13, 1989
Classifications
1
FEI Numbers
400
Registration Numbers
400
Same Product Code
725
Applicant Total
46
Review Days
110

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Basic Information

Device Name
CARDIAC OUTPUR/SATURATED VENOUS OXYGEN MODULE
K Number
K893867
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2700
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Spacelabs, Inc.
Date Received
May 26, 1989
Decision Date
September 13, 1989
Product Code
DQA
Advisory Committee
Cardiovascular
Review Advisory Committee
AN
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
DQA Oximeter

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K Number Device Name
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K950779 HEART RATE VARIABILITY SOFTWARE OPTION
K941165 COMET CAPNOGRAPH MODULE
K923788 SPACE LABS MODEL 90560
K912742 ESOPHAGEAL STETHOSCOPE TEMPERATURE PROBE
K913038 SPACELAB MODEL 90845 PCMS MULTIDISCLOSURE STATION
K905065 DEFIBRILLATOR LEAD ADAPTER
K910029 PATIENT CARE MANAGEMENT SYSTEM MODIFICATION
K896903 FIRST MEDIC MODEL 510
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