Cardon Rehabilitation Products, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Cardon Rehabilitation Products, Inc. - FDA 510(k) Cleared Devices
16
Total
16
Cleared
0
Denied
Cardon Rehabilitation Products, Inc. has 16 FDA 510(k) cleared physical medicine devices. Based in Niagara Falls, US.
Historical record: 16 cleared submissions from 1995 to 1996.
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 - Cardon Rehabilitation Products, Inc.
16 devices
Cleared
Feb 13, 1996
CARDON PHYSICAL THERAPY TABLE MODEL R28598
Physical Medicine
20d
Cleared
Feb 13, 1996
CARDON PHYSICAL THERAPY TABLE MODEL R27116
Physical Medicine
20d
Cleared
Feb 13, 1996
CARDON PHYSICAL THERAPY TABLE MODEL R27645
Physical Medicine
20d
Cleared
Jun 22, 1995
CARDON PHYSICAL THERAPY TABLE MODEL:R40194
Physical Medicine
57d
Cleared
Jun 15, 1995
CARDON PHYSICAL THERAPY TABLES MODELS R28591 & R28592
Physical Medicine
52d
Cleared
May 31, 1995
CARDON PHYSICAL THERAPY TABLE MODEL R27112
Physical Medicine
35d
Cleared
May 31, 1995
CARDON PHSICAL THERAPY TABLE MODEL R27630
Physical Medicine
35d
Cleared
May 31, 1995
CARDON PHYSICAL THERAPY TABLE MODEL R27108
Physical Medicine
35d
Cleared
May 25, 1995
CARDON PHYSICAL THERAPY TABLE MODEL: R27841
Physical Medicine
86d
Cleared
Apr 10, 1995
CARDON PHYSICAL THERAPY TABLES MODELS: R27622
Physical Medicine
41d
Cleared
Mar 14, 1995
CARDON PHYSICAL THERAPY TABLES MODELS: R27610
Physical Medicine
14d
Cleared
Feb 10, 1995
CARDON PHYSICAL THERAPY TABLE MODEL R28535
Physical Medicine
11d