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MODIFIED LEVEEN NEEDLE ELECTRODE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K962313
510(k) Type
Traditional
Applicant
RADIOTHERAPEUTICS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/11/1996
Days to Decision
86 days
Submission Type
Statement

MODIFIED LEVEEN NEEDLE ELECTRODE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K962313
510(k) Type
Traditional
Applicant
RADIOTHERAPEUTICS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/11/1996
Days to Decision
86 days
Submission Type
Statement