FDA 510(k) FDA class 2 Substantially Equivalent 🇩🇪 Germany

HEWLETT-PACKARD M1021A MIX VEN OXY SAT PLUG-IN MODULE

K Number: K942842 · Decision Feb 16, 1995
Classifications
1
FEI Numbers
400
Registration Numbers
400
Same Product Code
725
Applicant Total
16
Review Days
245

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Basic Information

Device Name
HEWLETT-PACKARD M1021A MIX VEN OXY SAT PLUG-IN MODULE
K Number
K942842
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2700
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Hewlett-Packard GmbH
Date Received
June 16, 1994
Decision Date
February 16, 1995
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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