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DIMAX 2

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K000771
510(k) Type
Traditional
Applicant
Planmeca Oy
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/3/2000
Days to Decision
55 days
Submission Type
Statement

DIMAX 2

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K000771
510(k) Type
Traditional
Applicant
Planmeca Oy
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/3/2000
Days to Decision
55 days
Submission Type
Statement