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

MODEL 192 PRINTER

K Number: K870538 · Decision Apr 23, 1987
Classifications
1
FEI Numbers
52
Registration Numbers
52
Same Product Code
86
Applicant Total
14
Review Days
73

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Basic Information

Device Name
MODEL 192 PRINTER
K Number
K870538
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
870.2810
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Advanced Medical Products, Inc.
Date Received
February 9, 1987
Decision Date
April 23, 1987
Product Code
DSF
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
DSF Recorder, Paper Chart

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K915658 SPECTRA ECG
K896103 MICRO FL 7400 AMBULATORY HOLTER/BP MONITOR
K896102 MICRO FD 7000 AMBULATORY BLOOD PRESSURE MONITOR
K881905 MODEL MICRO SI AMBULATORY ECG MONITOR
K872508 MODEL MICRO FD+ AMBULATORY ECG MONITOR
K870537 MODEL MICRO ST AMBULATORY ECG MONITOR
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