FDA Provides 510(k) Clearance for Software Modifications to STERIS System 1E Sterilization Device

STERIS Corp. has received FDA’s 510(k) clearance for software modifications to its System 1E liquid chemical sterilant processing system, according to a FDA report and a MEDCity report.

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By: Staff

 

The modifications address system aborts primarily caused by water-temperature issues.

 

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