Medical Device Manufacturer · US , Mchenry , IL

Kone Instruments, Inc. - FDA 510(k) Cleared Devices

12 submissions · 12 cleared · Since 1982

Total

Cleared

Denied

Kone Instruments, Inc. has 12 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 12 cleared submissions from 1982 to 1987. Primary specialty: Cardiovascular.

Browse the FDA 510(k) cleared devices submitted by Kone Instruments, Inc. Filter by specialty or product code using the sidebar.

Kone Instruments, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Kone Instruments, Inc.

12 devices

1-12 of 12

PROGRESS PLUS SELECTIVE CHEMISTRY ANALYZER

Cardiovascular · 105d

Cleared Aug 06, 1986

SIGNA II RESTING ECG ELECTRODE

K862655 · DRX

Cardiovascular · 23d

Cleared Apr 23, 1986

MODEL E 600 ELECTROCARDIOGRAPH

PROGRESS SELECTIVE DHEMISTRY ANALYZ

Kone Instruments, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Kone Instruments, Inc.

Filters