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APTIMAX INSTRUMENT TRAY, INSTRUMENT MAT AND INSTRUMENT HOLDER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K013003
510(k) Type
Traditional
Applicant
ADVANCED STERILIZATION PRODUCTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/28/2002
Days to Decision
356 days
Submission Type
Summary

APTIMAX INSTRUMENT TRAY, INSTRUMENT MAT AND INSTRUMENT HOLDER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K013003
510(k) Type
Traditional
Applicant
ADVANCED STERILIZATION PRODUCTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/28/2002
Days to Decision
356 days
Submission Type
Summary