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LEVEEN REFLECT MONOPOLAR/BIPOLAR NEEDLE ELECTRODE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K011220
510(k) Type
Traditional
Applicant
RADIOTHERAPEUTICS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/1/2002
Days to Decision
437 days
Submission Type
Summary

LEVEEN REFLECT MONOPOLAR/BIPOLAR NEEDLE ELECTRODE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K011220
510(k) Type
Traditional
Applicant
RADIOTHERAPEUTICS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/1/2002
Days to Decision
437 days
Submission Type
Summary