Central Line Dressing Change Tray

FDA 510(k) K941471 · Clinical Resources, Inc.

Substantially Equivalent

510(k) numberK941471

Submission

Device name
Central Line Dressing Change Tray
Applicant
Clinical Resources, Inc.
Elgin, IL, US
Received
March 28, 1994
Decision date
May 12, 1994
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
FRG – Wrap, Sterilization
Device class
Class II (moderate risk)
Regulation
21 CFR 880.6850
Specialty
General Hospital

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K252823Dukal Crepe Paper Sterilization WrapFRG · Traditional Dukal, LLC05/28/2026SE
K253454HALYARD* ONE-STEP* Sterilization Wrap; HALYARD* QUICK CHECK* Sterilization Wrap…FRG · Traditional O&M Halyard, Inc.05/18/2026SE
K251347Sterilization Pouch/RollFRG · Traditional Sterivic Medical Co., Ltd.01/28/2026SE
K251177Self-Seal Sterilization Pouch and RollFRG · Traditional Guangdong Maidi Medical Co., Ltd.12/12/2025SE
K250306Chex-All Sterilization Pouches and TubesFRG · Abbreviated Propper Manufacturing Co., Inc.10/31/2025SE
K243179Sterilization Pouch and RollFRG · Traditional Yichang Xinxin Paper Products Co., Ltd.06/26/2025SE
K250321GCI Sterilization WrappersFRG · Traditional George Courey, Inc.06/06/2025SE
K243721Self Sealing Sterilization PouchesFRG · Traditional Wellmed Dental Medical Supply Co., Ltd.04/25/2025SE
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More from Turbett Surgical

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K945021Fluff Gauze SpongeEFQ · Traditional 12/23/1994SE
K945020Fluff Gauze SpongeEFQ · Traditional 12/23/1994SE
K945019Fluff Gauxze RollEFQ · Traditional 12/23/1994SE
K944879Gauze SpongesGDY · Traditional 12/23/1994SE
K944880Bodily Fluid Disposal KitFXX · Traditional 12/15/1994SE
K941469IV Start KitLRS · Traditional 05/12/1994SE
K941468Debridement Tray, Incision and Drainage TrayFRG · Traditional 05/12/1994SE

Questions and answers

When was Central Line Dressing Change Tray cleared by the FDA?

Central Line Dressing Change Tray (K941471) received a 510(k) decision of Substantially Equivalent on May 12, 1994, 45 days after the submission was received.

What is the product code of K941471?

The FDA product code is FRG – Wrap, Sterilization, a Class II (moderate risk) device regulated under 21 CFR 880.6850.