Last synced on 14 November 2025 at 11:06 pm

STERILOX LIQUID CHEMICAL STERILANT SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K063159
510(k) Type
Traditional
Applicant
PURICORE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/2/2007
Days to Decision
167 days
Submission Type
Summary

STERILOX LIQUID CHEMICAL STERILANT SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K063159
510(k) Type
Traditional
Applicant
PURICORE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/2/2007
Days to Decision
167 days
Submission Type
Summary