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DU PONT LINX HD-25 LASR IMAGER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K923042
510(k) Type
Traditional
Applicant
E.I. DUPONT DE NEMOURS & CO., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/9/1992
Days to Decision
138 days
Submission Type
Summary

DU PONT LINX HD-25 LASR IMAGER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K923042
510(k) Type
Traditional
Applicant
E.I. DUPONT DE NEMOURS & CO., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/9/1992
Days to Decision
138 days
Submission Type
Summary