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LEVEEN NEEDLE ELECTRODE(TM)

Page Type
Cleared 510(K)
510(k) Number
K950347
510(k) Type
Traditional
Applicant
RADIOTHERAPEUTICS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/23/1995
Days to Decision
27 days
Submission Type
Statement

LEVEEN NEEDLE ELECTRODE(TM)

Page Type
Cleared 510(K)
510(k) Number
K950347
510(k) Type
Traditional
Applicant
RADIOTHERAPEUTICS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/23/1995
Days to Decision
27 days
Submission Type
Statement