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RADIAPAK BRACHYTHERAPY APPLICATOR BALLOON DEVICE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K120344
510(k) Type
Traditional
Applicant
Radiadyne, LLC (Specification Developer)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/3/2012
Days to Decision
90 days
Submission Type
Summary

RADIAPAK BRACHYTHERAPY APPLICATOR BALLOON DEVICE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K120344
510(k) Type
Traditional
Applicant
Radiadyne, LLC (Specification Developer)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/3/2012
Days to Decision
90 days
Submission Type
Summary