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23:1 REDUCTION ANGLE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K973800
510(k) Type
Traditional
Applicant
Midwest Dental Products Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/11/1998
Days to Decision
156 days
Submission Type
Statement

23:1 REDUCTION ANGLE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K973800
510(k) Type
Traditional
Applicant
Midwest Dental Products Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/11/1998
Days to Decision
156 days
Submission Type
Statement