510(k) K234132

Device
Medline Reusable Sterilization Wrappers
Applicant
Medline Industries, LP
510(k) number
K234132
Product code
FRG
Decision
Substantially Equivalent (SESE)
Decision date
2024-09-17
Date received
2023-12-28
Regulation
880.6850
Classification name
Wrap, Sterilization
Medical specialty
General Hospital
Review panel
General Hospital
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
N
Source
FDA openFDA 510(k) dataset plus migrated FDA.report data

Related Records

Applicant Contact

Contact
Closen Kelsey
Address
1 Three Lakes Dr. Northfield IL US 60093 60093

FDA Registration Numbers

Source Documents

FDA 510(k) Premarket Notification Database · 510(k) summary PDF · openFDA JSON

Other 510(k) Records For Product Code FRG

510(k)DeviceApplicantDecision date
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K241565Sterilization Package/ReelAnqing Clean Dental Instrument Technology Co., Ltd.2025-02-24
K243431Medicom Sterilization Pouch and ReelMedicom Asia-Pacific Holdings Ltd. Taiwan Branch.2025-02-21
K242898Sterilization Pouches and ReelsShanghai Jianzhong Medical Packaging Co., Ltd.2025-02-21
K240438CDB Hospital ® Sterilization Wrap (70 gsm); CDB Hospital ® Sterilization Wrap (44 gsm)Comercializadora Brever2024-11-04
K242839Safe Secure Sterilization Pouches and RollsShenzhen Safesecure Medical Infection Control Tech Co. , Ltd.2024-10-16
K242208PRIMED Sterilization Wrap (P100, P200, P300, P400, P500, P600)Primed Medical Products, Inc.2024-10-07
K241123Perpak™ Sterilization Tyvek PouchKm Corp.2024-09-18
K234050HALYARD® ONE-STEP® Sterilization Wrap, HALYARD® QUICK CHECK® Sterilization Wrap, HALYARD® SEQUENTIAL Sterilization Wrap and HALYARD® SMART-FOLD® Sterilization WrapO&M Halyard, Inc.2024-09-16