Parallax Medical, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Parallax Medical, Inc. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Parallax Medical, Inc. has 6 FDA 510(k) cleared medical devices. Based in Scotts Valley, US.
Historical record: 6 cleared submissions from 1999 to 2003. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Parallax Medical, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Parallax Medical, Inc.
6 devices
Cleared
Dec 12, 2003
TRACERS TA BONE CEMENT OPACIFIER, MODEL TCR-TA
Neurology
67d
Cleared
Mar 11, 2003
TRACERS BONE CEMENT OPACIFIER
Neurology
147d
Cleared
Jul 25, 2002
CLEARVIEW PLUS BONE AND VERTEBRAL BODY BIOPSY NEEDLES
Gastroenterology & Urology
22d
Cleared
Jul 18, 2001
PARALLAX BONE AND VERTEBRAL BODY BIOPSY AND INFUSION NEEDLES
Gastroenterology & Urology
90d
Cleared
Aug 31, 2000
PARALLAX CRANIOSET
Neurology
279d
Cleared
Aug 13, 1999
PARALLAX TRACER RADIOPAQUE PARTICLES
Neurology
71d