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RFA-300, LDA UTILITY

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K961400
510(k) Type
Traditional
Applicant
Scanditronix Medical AB
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/3/1997
Days to Decision
267 days
Submission Type
Summary

RFA-300, LDA UTILITY

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K961400
510(k) Type
Traditional
Applicant
Scanditronix Medical AB
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/3/1997
Days to Decision
267 days
Submission Type
Summary