đź“‹ FDA Reference

arrow vessel catheter kit w 20ga indwel

Arrow Intl.

Summary: The Arrow Vessel Catheter Kit is a medical device used for vascular access, primarily in venous procedures. It is commonly used by clinicians in settings such as hospitals and surgical centers.

FDA Clearance Information

Pathway 510K
Decision Date April 29, 1981
Product Code DQY
Device Class Class 2
Evidence 0 studies

The Arrow Vessel Catheter Kit by Arrow Intl. was cleared through the FDA 510k pathway on April 29, 1981. It is classified as a Class 2 device under product code DQY.

What It Is

The Arrow Vessel Catheter Kit includes a 20-gauge indwelling catheter designed for vascular access. It facilitates the insertion of a catheter into a vein, allowing for the administration of fluids, medications, or for venous pressure monitoring. The kit is typically used in procedures requiring reliable venous access.

Clinical Applications

This device is commonly used in clinical scenarios requiring venous access, such as in the administration of intravenous therapies, blood sampling, or central venous pressure monitoring. It is frequently utilized in emergency medicine, critical care, and surgical settings, catering to a wide range of patient populations from pediatric to adult.

Indications for Use

The FDA indications suggest this device is intended for use in patients needing venous access for therapeutic or diagnostic purposes. It is suitable for conditions requiring intravenous fluid administration or monitoring of venous pressure.

Practical Considerations

The catheter is typically available in a 20-gauge size, which is suitable for a variety of venous access needs. Clinicians should ensure compatibility with other intravenous equipment and be trained in proper insertion techniques to minimize complications.

Frequently Asked Questions

What is the Arrow Vessel Catheter Kit used for?

It is used for vascular access to administer fluids, medications, or monitor venous pressure.

What specialties typically use this device?

Specialties such as emergency medicine, critical care, and surgery commonly use this device.

What are the FDA-cleared indications?

The device is indicated for patients needing 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.

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