Medical Device Manufacturer · US , Netherlands

Ketronic, Inc. - FDA 510(k) Cleared Devices

10 submissions · 9 cleared · Since 1984

Total

Cleared

Denied

Ketronic, Inc. has 9 FDA 510(k) cleared physical medicine devices. Based in Netherlands, US.

Historical record: 9 cleared submissions from 1984 to 1985.

Browse the complete list of FDA 510(k) cleared physical medicine devices from this manufacturer. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Ketronic, Inc.

10 devices

1-10 of 10

Cleared Jun 12, 1985

MFE CARDIAC STRESS SYSTEM

K850868

Physical Medicine · 103d

Cleared Jun 12, 1985

MFE COUCH ERGOMETER

K850869 · ISD

Physical Medicine · 103d

Cleared Jun 12, 1985

MEDIFETTE ERGOMETER

K850870

Physical Medicine · 103d

Cleared Jun 12, 1985

HILO TABLES, TYPE CH-4, CH-8, FW-6, FW-5, FW-2, AL

K850873 · INO

Physical Medicine · 103d

Cleared Jun 12, 1985

MONOLIFT MPE2, PLATFORM, CHAIR, FULLY FUTO PLATFOR

K850877 · ILK

Physical Medicine · 103d

Cleared Jun 06, 1985

PHYACTION 300, 360, 370, 390 & 391 ELEC-MUSCLE-STI

K850872

Physical Medicine · 97d

Cleared Jun 05, 1985

TREDBAND TYPE I, IT, II & III - TREADMILLS

K850871 · BXB

Physical Medicine · 96d

Cleared May 16, 1985

ACTION-WHEELS & PLAY WHEELS

K850875

Physical Medicine · 76d

Cleared May 16, 1985

LIGTVOET L80.2 LIGHTFOOT L80.2 POWER WHEELCHAIR

K850876 · ITI

Physical Medicine · 76d

Ketronic, Inc. - FDA 510(k) Cleared Devices

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