đź“‹ FDA Reference

argyle intramedicut catheter kit

Sherwood Medical

Summary: The Argyle Intramedicut Catheter Kit is a medical device used primarily for vascular access in various clinical settings. It is commonly utilized by healthcare professionals in specialties such as interventional radiology and surgery.

FDA Clearance Information

Pathway 510K
Decision Date July 14, 1982
Product Code DYB
Device Class Class 2
Evidence 0 studies

The Argyle Intramedicut Catheter Kit was cleared through the FDA 510(k) pathway on July 14, 1982. Manufactured by Sherwood Medical, it is classified as a Class 2 device under product code DYB.

What It Is

The Argyle Intramedicut Catheter Kit is designed for vascular access, providing a means to introduce fluids, medications, or other devices into the bloodstream. It typically includes a catheter, needle, and other components necessary for insertion. This kit is essential for procedures requiring reliable venous access, such as intravenous therapy or diagnostic angiography.

Clinical Applications

This device is commonly used in interventional radiology, surgery, and emergency medicine. It is suitable for patients requiring long-term intravenous therapy, such as those undergoing chemotherapy or receiving nutritional support. The kit is also used in acute settings for rapid fluid resuscitation or medication administration.

Indications for Use

The FDA indications suggest that this device is intended for patients needing vascular access for therapeutic or diagnostic purposes. It is suitable for conditions requiring intravenous drug delivery or fluid management.

Practical Considerations

The Argyle Intramedicut Catheter Kit comes in various sizes to accommodate different patient anatomies and clinical needs. Compatibility with other vascular devices should be verified before use. Proper insertion technique is crucial to minimize complications such as infection or thrombosis.

Frequently Asked Questions

What is the Argyle Intramedicut Catheter Kit used for?

It is used for vascular access to administer fluids, medications, or for diagnostic purposes.

What specialties typically use this device?

Interventional radiology, surgery, and emergency medicine are the primary specialties using this device.

What are the FDA-cleared indications?

The device is indicated for patients requiring vascular access for therapeutic or diagnostic interventions.

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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