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curity venous catheterization kit
The Kendal
Summary: The Curity Venous Catheterization Kit is a medical device used for venous access. It is typically utilized by healthcare professionals in settings requiring intravenous therapy or monitoring.
FDA Clearance Information
Pathway
510K
Number
K861828 ↗
Decision Date
July 10, 1986
Product Code
DQY
Device Class
Class 2
Evidence
0 studies
The Curity Venous Catheterization Kit was cleared through the FDA 510k pathway on July 10, 1986. Manufactured by The Kendal, it is classified as a Class 2 device under product code DQY.
What It Is
The Curity Venous Catheterization Kit is designed to facilitate venous access for therapeutic or diagnostic purposes. It typically includes a catheter, needle, and other components necessary for safe and effective venous catheterization. This device is crucial in settings where intravenous access is needed, such as administering medications, fluids, or obtaining blood samples.
Clinical Applications
This device is commonly used in emergency departments, intensive care units, and surgical settings. It is vital for procedures requiring reliable venous access, such as fluid resuscitation, medication administration, and central venous pressure monitoring. The kit is suitable for a wide range of patient populations, including adults and pediatric patients, depending on the specific components and sizes available.
Indications for Use
The FDA-cleared indications for this device include establishing venous access for therapeutic or diagnostic purposes. It is intended for patients who require intravenous therapy, fluid management, or hemodynamic monitoring.
Practical Considerations
Clinicians should be aware of the various sizes and configurations available to match patient needs. Compatibility with other intravenous equipment should be considered, and proper aseptic technique is essential to minimize infection risk during catheterization.
Frequently Asked Questions
What is the Curity Venous Catheterization Kit used for?
The kit is used for establishing venous access for administering medications, fluids, or obtaining blood samples.
What specialties typically use this device?
Emergency medicine, critical care, anesthesiology, and surgery specialties commonly use this device.
What are the FDA-cleared indications?
The device is indicated for establishing venous access for therapeutic or diagnostic purposes.
Disclaimer: This page compiles publicly available regulatory and published clinical evidence for educational reference.
It does not constitute medical advice, product endorsement, or a recommendation for clinical use.
Always consult manufacturer documentation and clinical judgment for patient care decisions.