Medical Device Manufacturer · US , Cleveland , OH

Cleveland Medical Devices, Inc. - FDA 510(k) Cleared Devices

8 submissions · 8 cleared · Since 1995

Recent clearances: KINESIA, FAMILY OF CRYSTAL 20 MONITORS MODEL #CS20-600,900,1300,1400,2400 & 120, CRYSTAL MONITOR MODEL 16

View 8 510(k) Devices ↓

Total

Cleared

Denied

Cleveland Medical Devices, Inc. has 8 FDA 510(k) cleared medical devices. Based in Cleveland, US.

Historical record: 8 cleared submissions from 1995 to 2007. Primary specialty: Neurology.

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

Cleveland Medical Devices, Inc. is one of 20361 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Cleveland Medical Devices, Inc.

8 devices

1-8 of 8

FAMILY OF CRYSTAL 20 MONITORS MODEL #CS20-600,900,1300,1400,2400 & 120

K042039 · OLV

Neurology · 111d

Cleared Feb 19, 2002

CRYSTAL MONITOR MODEL 16

CRYSTAL-EEG MODEL 10 (MODEL 10)

Gastroenterology & Urology · 119d

Cleared Dec 04, 1996

FOOT WEIGHT ALARM

K962591 · IRN

Physical Medicine · 155d

Cleared Oct 30, 1995

PRESSORE MONITOR

K954670 · IKE

Physical Medicine · 20d

Cleveland Medical Devices, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Cleveland Medical Devices, Inc.

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