ClearanceBrief
Company ยท US

Cleveland Medical Devices, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 1995 to 2007. Name variants (Inc, Corp, punctuation) are merged.

8510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
OMCReduced- Montage Standard Electroencephalograph3
GYDTransducer, Tremor1
IKETransducer, Miniature Pressure1
IRNDevice, Warning, Overload, External Limb, Powered1
KNXCollector, Urine, (And Accessories) For Indwelling Catheter1
OLVStandard Polysomnograph With Electroencephalograph1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Apr 6, 2007K063872KINESIA
Cleveland Medical Devices, Inc.
GYD
Nov 17, 2004K042039FAMILY OF CRYSTAL 20 MONITORS MODEL #CS20-600,900,1300,1400,2400 & 120
Cleveland Medical Devices, Inc.
OLV
Feb 19, 2002K013863CRYSTAL MONITOR MODEL 16
Cleveland Medical Devices, Inc.
OMC
Jul 5, 2000K001110CRYSTAL-EEG MODEL 15
Cleveland Medical Devices, Inc.
OMC
May 22, 1997K970672CRYSTAL-EEG MODEL 10 (MODEL 10)
Cleveland Medical Devices, Inc.
OMC
Mar 21, 1997K964690LIBERTY VALVE
Cleveland Medical Devices, Inc.
KNX
Dec 4, 1996K962591FOOT WEIGHT ALARM
Cleveland Medical Devices, Inc.
IRN
Oct 30, 1995K954670PRESSORE MONITOR
Cleveland Medical Devices, Inc.
IKE

Latest recalls

DateFirm and productCodeLinked 510(k)
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