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Kone Instruments, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
12
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K873345'MICROLYTE 4/5'September 11, 1987
K870777PROGRESS PLUS SELECTIVE CHEMISTRY ANALYZERMarch 13, 1987
K863466M700 STRESS MONITORDecember 22, 1986
K862655SIGNA II RESTING ECG ELECTRODEAugust 6, 1986
K860767MODEL E 600 ELECTROCARDIOGRAPHApril 23, 1986
K853354MEDIC 4October 11, 1985
K840200PROGRESS SELECTIVE DHEMISTRY ANALYZApril 4, 1984
K830432CENTRAL STATION 590March 24, 1983
K830433PATIENT MONITOR 575March 24, 1983
K822952560November 1, 1982
K820541MICROLYTEMay 24, 1982
K820540OLLI 565April 1, 1982