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RADIOTHERAPEUTICS RF 3000 RADIOFREQUENCY GENERATOR

Page Type
Cleared 510(K)
510(k) Number
K000241
510(k) Type
Traditional
Applicant
RADIOTHERAPEUTICS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/14/2000
Days to Decision
78 days
Submission Type
Statement

RADIOTHERAPEUTICS RF 3000 RADIOFREQUENCY GENERATOR

Page Type
Cleared 510(K)
510(k) Number
K000241
510(k) Type
Traditional
Applicant
RADIOTHERAPEUTICS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/14/2000
Days to Decision
78 days
Submission Type
Statement