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PRO-LITE Sterilization Tray

Page Type
Cleared 510(K)
510(k) Number
K183301
510(k) Type
Traditional
Applicant
STERIS Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/3/2019
Days to Decision
37 days
Submission Type
Summary

PRO-LITE Sterilization Tray

Page Type
Cleared 510(K)
510(k) Number
K183301
510(k) Type
Traditional
Applicant
STERIS Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/3/2019
Days to Decision
37 days
Submission Type
Summary