Rita Medical Systems, Inc. is one of 24542 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Rita Medical Systems, Inc. - FDA 510(k) Cleared Devices
Recent clearances: UNIBLATE ELECTROSURGICAL DEVICE, VORTEX CT PORT ACCESS SYSTEM AND LIFEGUARD SAFETY INFUSION SET, OMNIPICC P.I.
9
Total
9
Cleared
0
Denied
Rita Medical Systems, Inc. has 9 FDA 510(k) cleared medical devices. Based in Mountain View, US.
Historical record: 9 cleared submissions from 2003 to 2007. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Rita Medical Systems, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Underwriters Laboratories, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Rita Medical Systems, Inc.
9 devices
Cleared
Feb 14, 2007
UNIBLATE ELECTROSURGICAL DEVICE
General & Plastic Surgery
35d
Cleared
Feb 01, 2007
VORTEX CT PORT ACCESS SYSTEM AND LIFEGUARD SAFETY INFUSION SET
General Hospital
168d
Cleared
Nov 28, 2006
OMNIPICC P.I.
General Hospital
89d
Cleared
Nov 23, 2005
OMNIPICC PI
General Hospital
208d
Cleared
Feb 25, 2005
VORTEX EZ VASCULAR ACCESS PORT
General Hospital
30d
Cleared
Sep 09, 2003
RITA MODEL 1500X ELECTROSURGICAL RF GENERATOR
General & Plastic Surgery
57d
Cleared
Jul 17, 2003
RITA MODEL 1500X ELECTROSURGICAL RF GENERATOR AND ACCESSORIES (E.G., RITA...
General & Plastic Surgery
24d
Cleared
May 02, 2003
RITA MODEL 1500X ELECTROSURGICAL RF GENERATOR
General & Plastic Surgery
11d
Cleared
Apr 01, 2003
RITA CLIPS FOR INFUSION PUMPS
General Hospital
7d