The following data is part of a premarket notification filed by Standard Textile Co., Inc. with the FDA for Standard Supreme Sterilization Wrapper.
Device ID | K172207 |
510k Number | K172207 |
Device Name: | Standard Supreme Sterilization Wrapper |
Classification | Wrap, Sterilization |
Applicant | Standard Textile Co., Inc. One Knollcrest Drive Cincinnati, OH 45237 |
Contact | Bradley J. Bushman |
Correspondent | Jonathan Kahan Hogan Lovells US LLP 555 Thirteenth Street, NW Washington, DC 20004 -1109 |
Product Code | FRG |
CFR Regulation Number | 880.6850 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2017-07-21 |
Decision Date | 2017-08-25 |
Summary: | summary |