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

CDI 100 EXTRACORPOREAL HEMATOCRIT/OXYGEN SATURATIO

K Number: K931968 · Decision Nov 10, 1993
Classifications
1
FEI Numbers
21
Registration Numbers
21
Same Product Code
46
Applicant Total
49
Review Days
203

Basic Information

Device Name
CDI 100 EXTRACORPOREAL HEMATOCRIT/OXYGEN SATURATIO
K Number
K931968
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.4330
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
3M HEALTH CARE, LTD.
Date Received
April 21, 1993
Decision Date
November 10, 1993
Product Code
DRY
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
DRY Monitor, Blood-Gas, On-Line, Cardiopulmonary Bypass

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