Last synced on 12 August 2022 at 11:05 pm

DURALIFE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K922537
510(k) Type
Traditional
Applicant
DHD DIEMOLDING HEALTHCARE DIV.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/4/1992
Days to Decision
190 days
Submission Type
Statement

DURALIFE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K922537
510(k) Type
Traditional
Applicant
DHD DIEMOLDING HEALTHCARE DIV.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/4/1992
Days to Decision
190 days
Submission Type
Statement