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VERIFY SixCess Steam Indicators, VERIFY SixCess Flash Indicators, VERIFY Bowie Dick Test Pack, VERIFY SixCess Challenge Pack, VERIFY SixCess FP Challenge Pack

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K162758
510(k) Type
Traditional
Applicant
STERIS Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/21/2017
Days to Decision
172 days
Submission Type
Summary

VERIFY SixCess Steam Indicators, VERIFY SixCess Flash Indicators, VERIFY Bowie Dick Test Pack, VERIFY SixCess Challenge Pack, VERIFY SixCess FP Challenge Pack

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K162758
510(k) Type
Traditional
Applicant
STERIS Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/21/2017
Days to Decision
172 days
Submission Type
Summary