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

APPLISCOPE

K Number: K864978 · Decision Feb 19, 1987
Classifications
1
FEI Numbers
177
Registration Numbers
177
Same Product Code
574
Applicant Total
8
Review Days
59

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Basic Information

Device Name
APPLISCOPE
K Number
K864978
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2340
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Grandcor Medical Systems
Date Received
December 22, 1986
Decision Date
February 19, 1987
Product Code
DPS
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
DPS Electrocardiograph

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Other Clearances by Grandcor Medical Systems

K Number Device Name
K905480 SPIROSCOPE
K895547 GRANDCOR/CARDIOLINE ECT STRESS TESTING
K883410 CARDIOMEGA-T
K871890 CARDIO-MEGA SYSTEM
K864260 APPLICARD SYSTEM (ECG ELECTRODE SYSTEM)
K864581 APPLIDYN
K862375 CARDIO PORT 500 24-H ECG AMBULATORY MONITOR SYSTEM