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Company · US

Kone Instruments, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 1982 to 1987. Name variants (Inc, Corp, punctuation) are merged.

12510(k) clearances (0 in 12 months)

0recalls (0 in 12 months)

0recalls that name a 510(k)

Product codes

Code	Device	Records
DRT	Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)	5
JJF	Analyzer, Chemistry, Micro, For Clinical Use	3
DRX	Electrode, Electrocardiograph	1
DSI	Detector And Alarm, Arrhythmia	1
JFP	Electrode, Ion Specific, Calcium	1
LDD	Dc-Defibrillator, Low-Energy, (Including Paddles)	1

Latest 510(k) clearances

Decided	510(k)	Device and applicant	Code
Sep 11, 1987	K873345	'MICROLYTE 4/5' Kone Instruments, Inc.	JFP
Mar 13, 1987	K870777	PROGRESS PLUS SELECTIVE CHEMISTRY ANALYZER Kone Instruments, Inc.	JJF
Dec 22, 1986	K863466	M700 STRESS MONITOR Kone Instruments, Inc.	DRT
Aug 6, 1986	K862655	SIGNA II RESTING ECG ELECTRODE Kone Instruments, Inc.	DRX
Apr 23, 1986	K860767	MODEL E 600 ELECTROCARDIOGRAPH Kone Instruments, Inc.	DSI
Oct 11, 1985	K853354	MEDIC 4 Kone Instruments, Inc.	LDD
Apr 4, 1984	K840200	PROGRESS SELECTIVE DHEMISTRY ANALYZ Kone Instruments, Inc.	JJF
Mar 24, 1983	K830433	PATIENT MONITOR 575 Kone Instruments, Inc.	DRT
Mar 24, 1983	K830432	CENTRAL STATION 590 Kone Instruments, Inc.	DRT
Nov 1, 1982	K822952	560 Kone Instruments, Inc.	DRT
May 24, 1982	K820541	MICROLYTE Kone Instruments, Inc.	JJF
Apr 1, 1982	K820540	OLLI 565 Kone Instruments, Inc.	DRT

Latest recalls

Date	Firm and product	Code	Linked 510(k)
No recalls in this window.

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