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DURALIFE(TM)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K913726
510(k) Type
Traditional
Applicant
DHD DIEMOLDING HEALTHCARE DIV.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/7/1992
Days to Decision
171 days
Submission Type
Statement

DURALIFE(TM)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K913726
510(k) Type
Traditional
Applicant
DHD DIEMOLDING HEALTHCARE DIV.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/7/1992
Days to Decision
171 days
Submission Type
Statement