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DURALIFE(TM)

Page Type
Cleared 510(K)
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)
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