Radiotherapeutics Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Radiotherapeutics Corp. - FDA 510(k) Cleared Devices
12
Total
11
Cleared
0
Denied
Radiotherapeutics Corp. has 11 FDA 510(k) cleared general & plastic surgery devices. Based in Mountain View, US.
Historical record: 11 cleared submissions from 1995 to 2002.
Browse the complete list of FDA 510(k) cleared general & plastic surgery devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Radiotherapeutics Corp.
12 devices
Cleared
Jul 01, 2002
LEVEEN REFLECT MONOPOLAR/BIPOLAR NEEDLE ELECTRODE
General & Plastic Surgery
437d
Cleared
Oct 11, 2001
LEVEEN ELECTRODE
General & Plastic Surgery
80d
Cleared
Apr 14, 2000
RADIOTHERAPEUTICS RF 3000 RADIOFREQUENCY GENERATOR
General & Plastic Surgery
78d
Cleared
Apr 06, 2000
LEVEEN NEEDLE ELECTRODE
General & Plastic Surgery
624d
Cleared
Mar 30, 2000
LEVEEN NEEDLE ELECTRODE
General & Plastic Surgery
85d
Cleared
Nov 10, 1998
MR COMPATIBLE LEVEEN NEEDLE ELECTRODE
General & Plastic Surgery
89d
Cleared
Jul 17, 1998
RADIOTHERAPEUTICS RF-2000 RADIOFREQUENCY GENERATOR
General & Plastic Surgery
66d
Cleared
Sep 04, 1997
RADIOTHERAPEUTICS RF GENERATOR. MODEL #RF-2000
General & Plastic Surgery
66d
Cleared
Sep 11, 1996
MODIFIED LEVEEN NEEDLE ELECTRODE
General & Plastic Surgery
86d
Cleared
Aug 20, 1996
SENSOR SHEATH TS1
General Hospital
61d
Cleared
Apr 07, 1996
RADIOTHERAPEUTICS RF GENERATOR MODEL RF-1000
General & Plastic Surgery
146d
Cleared
Feb 23, 1995
LEVEEN NEEDLE ELECTRODE(TM)
General & Plastic Surgery
27d