Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links
  • Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

510(k) Premarket Notification
  • Print
  • Share
  • E-mail
-
Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 


New Search Back To Search Results
Device Classification Name Indicator, Physical/Chemical Sterilization Process
510(k) Number K173428
Device Name VERIFY Chemical Indicator for S40 Sterilant
Applicant
STERIS Corporation
5976 Heisley Rd.
Mentor,  OH  44060
Applicant Contact Marcia L. Benedict
Correspondent
STERIS Corporation
5976 Heisley Rd.
Mentor,  OH  44060
Correspondent Contact Marcia L. Benedict
Regulation Number880.2800
Classification Product Code
JOJ  
Date Received11/02/2017
Decision Date 03/02/2018
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General Hospital
510k Review Panel General Hospital
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-