Camtronics, Ltd. is one of 5771 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Camtronics, Ltd. - FDA 510(k) Cleared Devices
Recent clearances: SURGERY AND ACCESSORIES, PHYSIOLOG, SERIES 95000, VIDEO PLUS SYSTEM, SERIES 95000
16
Total
16
Cleared
0
Denied
Camtronics, Ltd. has 16 FDA 510(k) cleared radiology devices. Based in Delafield, US.
Historical record: 16 cleared submissions from 1987 to 2002.
Browse the complete list of FDA 510(k) cleared radiology devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Camtronics, Ltd.
16 devices
Cleared
Jul 17, 2002
SURGERY AND ACCESSORIES
Radiology
90d
Cleared
Jun 04, 2002
PHYSIOLOG, SERIES 95000
Cardiovascular
267d
Cleared
Oct 13, 1999
VIDEO PLUS SYSTEM, SERIES 95000
Radiology
65d
Cleared
Sep 08, 1999
ECHOCARDIOGRAPHY SYSTEM SERIES 95000
Radiology
64d
Cleared
Mar 17, 1999
CCD CAMERA, MODEL 9000
Radiology
68d
Cleared
May 09, 1996
ANALYTICAL REVIEW STATION
Radiology
157d
Cleared
Mar 19, 1996
DIGITAL IMAGING SYSTEM
Radiology
196d
Cleared
Dec 11, 1995
NT SERIES DIGITAL IMAGE MANAGER
Radiology
27d
Cleared
Sep 28, 1995
DIGITAL IMAGING SYSTEM INTERFACE
Radiology
87d
Cleared
Feb 17, 1995
NICOM DIGITAL IMAGE MANAGER
Radiology
92d
Cleared
Aug 17, 1994
VIDEO PLUS WITH ANALYTICAL WORKSTATION
Radiology
114d
Cleared
Dec 13, 1993
X-RAY ANGIOGRAPHIC SYSTEM
Radiology
89d