FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

CPE 2000 CARDIO PULMONARY ERGOMETER

K Number: K874925 · Decision Jan 19, 1988
Classifications
1
FEI Numbers
48
Registration Numbers
48
Same Product Code
41
Applicant Total
23
Review Days
48

Basic Information

Device Name
CPE 2000 CARDIO PULMONARY ERGOMETER
K Number
K874925
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
870.4200
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
MEDICAL GRAPHICS CORP.
Date Received
December 2, 1987
Decision Date
January 19, 1988
Product Code
KRI
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
KRI Accessory Equipment, Cardiopulmonary Bypass

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