The following data is part of a premarket notification filed by Steris Corporations with the FDA for Verify V24 Self-contained Biological Indicator, Verify V24 Biological Indicator Challenge Pack.
Device ID | K172748 |
510k Number | K172748 |
Device Name: | VERIFY V24 Self-Contained Biological Indicator, VERIFY V24 Biological Indicator Challenge Pack |
Classification | Indicator, Biological Sterilization Process |
Applicant | STERIS Corporations 5960 Heisley Road Mentor, OH 44060 |
Contact | Jennifer Nalepka |
Correspondent | Jennifer Nalepka STERIS Corporations 5960 Heisley Road Mentor, OH 44060 |
Product Code | FRC |
CFR Regulation Number | 880.2800 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2017-09-12 |
Decision Date | 2018-02-09 |
Summary: | summary |