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FDA 510(k) Applications Submitted by RADIOTHERAPEUTICS CORP.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K981672
05/12/1998
RADIOTHERAPEUTICS RF-2000 RADIOFREQUENCY GENERATOR
RADIOTHERAPEUTICS CORP.
K962313
06/17/1996
MODIFIED LEVEEN NEEDLE ELECTRODE
RADIOTHERAPEUTICS CORP.
K962386
06/20/1996
SENSOR SHEATH TS1
RADIOTHERAPEUTICS CORP.
K972441
06/30/1997
RADIOTHERAPEUTICS RF GENERATOR. MODEL #RF-2000
RADIOTHERAPEUTICS CORP.
K982556
07/22/1998
LEVEEN NEEDLE ELECTRODE
RADIOTHERAPEUTICS CORP.
K982854
08/13/1998
MR COMPATIBLE LEVEEN NEEDLE ELECTRODE
RADIOTHERAPEUTICS CORP.
K955144
11/13/1995
RADIOTHERAPEUTICS RF GENERATOR MODEL RF-1000
RADIOTHERAPEUTICS CORP.
K000032
01/05/2000
LEVEEN NEEDLE ELECTRODE
RADIOTHERAPEUTICS CORP.
K000241
01/27/2000
RADIOTHERAPEUTICS RF 3000 RADIOFREQUENCY GENERATOR
RADIOTHERAPEUTICS CORP.
K011220
04/20/2001
LEVEEN REFLECT MONOPOLAR/BIPOLAR NEEDLE ELECTRODE
RADIOTHERAPEUTICS CORP.
K012315
07/23/2001
LEVEEN ELECTRODE
RADIOTHERAPEUTICS CORP.
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