High Dose Disconnect Cap and Minicap with Povidone-Iodine, High Dose Disconnect Cap with Povidone-Iodine

FDA 510(k) K972579 · Baxter Healthcare Corp

Substantially Equivalent

510(k) numberK972579

Submission

Device name
High Dose Disconnect Cap and Minicap with Povidone-Iodine, High Dose Disconnect Cap with Povidone-Iodine
Applicant
Baxter Healthcare Corp
Mcgaw Park, IL, US
Received
July 10, 1997
Decision date
October 1, 1997
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
KDJ – Set, Administration, For Peritoneal Dialysis, Disposable
Device class
Class II (moderate risk)
Regulation
21 CFR 876.5630
Specialty
Gastroenterology, Urology
Life-sustaining
Yes

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K173593stay•safe catheter extension set with Safe-Lock, 12 inch, stay•safe catheter extension…KDJ · Traditional Fresenius Medical Care Renal Therapies Group, LLC05/21/2018SE
K173651Multiple Tubing Segment Set with stay safe PIN Connectors, stay safe Drain SetKDJ · Traditional Fresenius Medical Care Renal Therapies Group, LLC02/14/2018SE
K173363Cycler Drain Bag SetKDJ · Traditional Fresenius Medical Care Renal Therapies Group, LLC01/24/2018SE
K151620Firefly Peritoneal Dialysis Connector Disinfection SystemKDJ · Traditional Puracath Medical, Inc.01/20/2016SE
K152675Extended Life Capd Transfer Set, Peritoneal Dialysis Titanium Catheter Adapter and…KDJ · Traditional Baxter Healthcare10/29/2015SE
K152129FlexiCap Disconnect Cap with Povidone-Iodine Solution, MiniCap with Povidone-Iodine…KDJ · Traditional Baxter Healthcare Corporation10/29/2015SE

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K230665Dose IQ Safety SoftwarePHC · Traditional 03/29/2024SE
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Questions and answers

When was High Dose Disconnect Cap and Minicap with Povidone-Iodine, High Dose Disconnect Cap with Povidone-Iodine cleared by the FDA?

High Dose Disconnect Cap and Minicap with Povidone-Iodine, High Dose Disconnect Cap with Povidone-Iodine (K972579) received a 510(k) decision of Substantially Equivalent on October 1, 1997, 83 days after the submission was received.

What is the product code of K972579?

The FDA product code is KDJ – Set, Administration, For Peritoneal Dialysis, Disposable, a Class II (moderate risk) device regulated under 21 CFR 876.5630.