Sterile Saline for Catheter Care

FDA 510(k) K974397 · Baxter Healthcare Corp

Substantially Equivalent

510(k) numberK974397

Submission

Device name
Sterile Saline for Catheter Care
Applicant
Baxter Healthcare Corp
Round Lake, IL, US
Received
November 21, 1997
Decision date
February 10, 1998
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
JOL – Catheter And Tip, Suction
Device class
Class II (moderate risk)
Regulation
21 CFR 880.6740
Specialty
General Hospital

Other 510(k)s with product code JOL

510(k)DeviceApplicantDecision
K051370Sterile Saline for Device Care, Sterile Water for Device Care, Models 2F7121, 2F8014JOL · Traditional Baxter Healthcare Corp08/12/2005SE
K000266Primary Care Solutions Sterile SALINE-0.9% Sodium Chloride for Device IrrigationJOL · Traditional Primary Care Solutions, Inc.07/12/2001SE
K000265Primary Care Solutions Sterile Water Device IrrigationJOL · Traditional Primary Care Solutions, Inc.07/12/2001SE
K003402Welcon Sterile Water for Device Irrigation; Welcon Sterile 0.9% Normal Saline for Device…JOL · Traditional Welcon, Inc.05/01/2001SE
K994321Sterile Water and 0.9% Sodium Chloride for Irrigation, UspJOL · Traditional Automatic Liquid Packaging, Inc.10/25/2000SE
K974759Hydrox Saline Solution 0.9% Sodium Chloride 4 Oz. Cup 120 ML 100 ML BottleJOL · Traditional Hydrox Laboratories03/09/1998SE
K974758Hydrox Sterile Water 4 Oz. Cup 120 Ml., Hydrox Sterile Water 100 ML BottleJOL · Traditional Hydrox Laboratories03/09/1998SE
K973734Sterile Water for Device Irrigation/ Sterile Saline for Device IrrigationJOL · Traditional Welcon, Inc.02/05/1998SE
K972372Germ Trapper Suction Tube HolderJOL · Traditional Rzv Medical Specialties, Inc.12/11/1997SE
K960216CPR Suction Catheter KitJOL · Traditional Custom Pack Reliability04/15/1996SE

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Questions and answers

When was Sterile Saline for Catheter Care cleared by the FDA?

Sterile Saline for Catheter Care (K974397) received a 510(k) decision of Substantially Equivalent on February 10, 1998, 81 days after the submission was received.

What is the product code of K974397?

The FDA product code is JOL – Catheter And Tip, Suction, a Class II (moderate risk) device regulated under 21 CFR 880.6740.