FDA 510(k) Applications Submitted by CLEVELAND MEDICAL DEVICES, INC.

FDA 510(k) Number Submission Date Device Name Applicant
K063872 12/29/2006 KINESIA CLEVELAND MEDICAL DEVICES, INC.
K970672 02/24/1997 CRYSTAL-EEG MODEL 10 (MODEL 10) CLEVELAND MEDICAL DEVICES, INC.
K001110 04/06/2000 CRYSTAL-EEG MODEL 15 CLEVELAND MEDICAL DEVICES, INC.
K962591 07/02/1996 FOOT WEIGHT ALARM CLEVELAND MEDICAL DEVICES, INC.
K042039 07/29/2004 FAMILY OF CRYSTAL 20 MONITORS MODEL #CS20-600,900,1300,1400,2400 & 120 CLEVELAND MEDICAL DEVICES, INC.
K013863 11/21/2001 CRYSTAL MONITOR MODEL 16 CLEVELAND MEDICAL DEVICES, INC.
K964690 11/22/1996 LIBERTY VALVE CLEVELAND MEDICAL DEVICES, INC.


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