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

MODEL MPA MULTI PARAMETER ANALYSIS MONITORING SYS.

K Number: K871990 · Decision Oct 7, 1987
Classifications
1
FEI Numbers
24
Registration Numbers
24
Same Product Code
35
Applicant Total
48
Review Days
134

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Basic Information

Device Name
MODEL MPA MULTI PARAMETER ANALYSIS MONITORING SYS.
K Number
K871990
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.1400
Medical Specialty
Neurology
Decision
Substantially Equivalent
Applicant
Oxford Medilog, Inc.
Date Received
May 26, 1987
Decision Date
October 7, 1987
Product Code
OLZ
Advisory Committee
Neurology
Review Advisory Committee
NE
Third Party
N

Classifications

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

Product Code Device Name
OLZ Automatic Event Detection Software For Polysomnograph With Electroencephalograph

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