The following data is part of a premarket notification filed by Cardinal Health 200, Llc with the FDA for Dura Blue Sterilization Wrap.
Device ID | K112283 |
510k Number | K112283 |
Device Name: | DURA BLUE STERILIZATION WRAP |
Classification | Wrap, Sterilization |
Applicant | CARDINAL HEALTH 200, LLC 1430 WAUKEGAAN ROAD Waukegan, IL 60085 |
Contact | Lavenia Ford |
Correspondent | Ned Devine UNDERWRITERS LABORATORIES, INC. 333 PFINGSTEN RD. Northbrook, IL 60062 |
Product Code | FRG |
CFR Regulation Number | 880.6850 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | Yes |
Combination Product | No |
Date Received | 2011-08-09 |
Decision Date | 2011-10-20 |
Summary: | summary |