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Radiotherapeutics Corp.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
12
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K011220LEVEEN REFLECT MONOPOLAR/BIPOLAR NEEDLE ELECTRODEJuly 1, 2002
K012315LEVEEN ELECTRODEOctober 11, 2001
K000241RADIOTHERAPEUTICS RF 3000 RADIOFREQUENCY GENERATORApril 14, 2000
K982556LEVEEN NEEDLE ELECTRODEApril 6, 2000
K000032LEVEEN NEEDLE ELECTRODEMarch 30, 2000
K982854MR COMPATIBLE LEVEEN NEEDLE ELECTRODENovember 10, 1998
K981672RADIOTHERAPEUTICS RF-2000 RADIOFREQUENCY GENERATORJuly 17, 1998
K972441RADIOTHERAPEUTICS RF GENERATOR. MODEL #RF-2000September 4, 1997
K962313MODIFIED LEVEEN NEEDLE ELECTRODESeptember 11, 1996
K962386SENSOR SHEATH TS1August 20, 1996
K955144RADIOTHERAPEUTICS RF GENERATOR MODEL RF-1000April 7, 1996
K950347LEVEEN NEEDLE ELECTRODE(TM)February 23, 1995