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

SAMS 8000 CARDIOPLEGIA MONITOR

K Number: K960916 · Decision Jun 4, 1996
Classifications
1
FEI Numbers
39
Registration Numbers
39
Same Product Code
5
Applicant Total
76
Review Days
90

Basic Information

Device Name
SAMS 8000 CARDIOPLEGIA MONITOR
K Number
K960916
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1100
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
3M HEALTH CARE, SARNS
Date Received
March 6, 1996
Decision Date
June 4, 1996
Product Code
DSJ
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
DSJ Alarm, Blood-Pressure

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