Last synced on 25 January 2026 at 3:41 am

MINIBLASTER

Page Type
Cleared 510(K)
PDF
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
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