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MINIBLASTER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K013969
510(k) Type
Traditional
Applicant
DELDENT LTD.
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
1/10/2002
Days to Decision
38 days
Submission Type
Statement

MINIBLASTER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K013969
510(k) Type
Traditional
Applicant
DELDENT LTD.
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
1/10/2002
Days to Decision
38 days
Submission Type
Statement