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

MEDIC 4

K Number: K853354 · Decision Oct 11, 1985
Classifications
1
FEI Numbers
36
Registration Numbers
36
Same Product Code
165
Applicant Total
12
Review Days
60

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Basic Information

Device Name
MEDIC 4
K Number
K853354
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.5300
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Kone Instruments, Inc.
Date Received
August 12, 1985
Decision Date
October 11, 1985
Product Code
LDD
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
LDD Dc-Defibrillator, Low-Energy, (Including Paddles)

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Other Clearances by Kone Instruments, Inc.

K Number Device Name
K873345 'MICROLYTE 4/5'
K870777 PROGRESS PLUS SELECTIVE CHEMISTRY ANALYZER
K863466 M700 STRESS MONITOR
K862655 SIGNA II RESTING ECG ELECTRODE
K860767 MODEL E 600 ELECTROCARDIOGRAPH
K840200 PROGRESS SELECTIVE DHEMISTRY ANALYZ
K830433 PATIENT MONITOR 575
K830432 CENTRAL STATION 590
K822952 560
K820541 MICROLYTE
Search all 12 clearances from Kone Instruments, Inc. →