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

DATA RECORDER

K Number: K910118 · Decision Feb 14, 1991
Classifications
1
FEI Numbers
488
Registration Numbers
488
Same Product Code
797
Applicant Total
35
Review Days
34

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Basic Information

Device Name
DATA RECORDER
K Number
K910118
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.2910
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Healthdyne, Inc.
Date Received
January 11, 1991
Decision Date
February 14, 1991
Product Code
FLL
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

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

Product Code Device Name
FLL Continuous Measurement Thermometer

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K922623 NEBULIZER SYSTEM
K903287 MODEL 900S APNEA/HEART MONITOR
K894030 MODEL 37 UTERINE CONTRACTION ACTIVITY MONITOR
K892006 HEALTHDYNE'S APNEA/HEART MONITOR, MODEL 900S
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