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OCENTRA MASTERPLAN 3.1 (OCENTRA BRACHY)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K081281
510(k) Type
Traditional
Applicant
NUCLETRON CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/20/2008
Days to Decision
14 days
Submission Type
Summary

OCENTRA MASTERPLAN 3.1 (OCENTRA BRACHY)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K081281
510(k) Type
Traditional
Applicant
NUCLETRON CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/20/2008
Days to Decision
14 days
Submission Type
Summary