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LEVEEN NEEDLE ELECTRODE

Page Type
Cleared 510(K)
510(k) Number
K000032
510(k) Type
Traditional
Applicant
Radiotherapeutics Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/30/2000
Days to Decision
85 days
Submission Type
Statement

LEVEEN NEEDLE ELECTRODE

Page Type
Cleared 510(K)
510(k) Number
K000032
510(k) Type
Traditional
Applicant
Radiotherapeutics Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/30/2000
Days to Decision
85 days
Submission Type
Statement