The following data is part of a premarket notification filed by Medline Industries, Inc. with the FDA for Medline Sharps Containers.
Device ID | K143693 |
510k Number | K143693 |
Device Name: | MEDLINE SHARPS CONTAINERS |
Classification | Container, Sharps |
Applicant | MEDLINE INDUSTRIES, INC. ONE MEDLINE PLACE Mundlelein, IL 60060 |
Contact | Matt Clausen |
Correspondent | Matt Clausen MEDLINE INDUSTRIES, INC. ONE MEDLINE PLACE Mundlelein, IL 60060 |
Product Code | MMK |
CFR Regulation Number | 880.5570 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2014-12-24 |
Decision Date | 2015-11-06 |
Summary: | summary |