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

MODIFIED DR-2C/PMC 100

K Number: K896153 · Decision Jan 19, 1990
Classifications
1
FEI Numbers
56
Registration Numbers
56
Same Product Code
193
Applicant Total
13
Review Days
87

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Basic Information

Device Name
MODIFIED DR-2C/PMC 100
K Number
K896153
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2800
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
General Devices
Date Received
October 24, 1989
Decision Date
January 19, 1990
Product Code
DSH
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
DSH Recorder, Magnetic Tape, Medical

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K921929 GEMSCOM SERIES 300 12-LEAD ECG (12-LEAD OPTION)
K914889 GEMSCOM SERIES 3000
K912008 TRU-VIEW MULTI-CHANNEL DISPLAY
K862596 DR-2C (MODIFICATION)
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