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MODIFICATION TO RESERT XL HLD HIGH LEVEL DISINFECTANT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K091022
510(k) Type
Traditional
Applicant
STERIS Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/12/2010
Days to Decision
368 days
Submission Type
Summary

MODIFICATION TO RESERT XL HLD HIGH LEVEL DISINFECTANT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K091022
510(k) Type
Traditional
Applicant
STERIS Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/12/2010
Days to Decision
368 days
Submission Type
Summary