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implant pacing lead tined 3262 modification
Oscor Medical
Summary: The implant pacing lead tined 3262 by Oscor Medical is a cardiac device used for pacing the heart. It is primarily used by cardiologists in patients requiring cardiac pacing.
FDA Clearance Information
Pathway
510K
Number
K913202 ↗
Decision Date
September 23, 1991
Product Code
DTB
Device Class
Class 3
Evidence
0 studies
The implant pacing lead tined 3262 was cleared through the FDA 510(k) pathway on September 23, 1991. Manufactured by Oscor Medical, it is classified as a Class III device.
What It Is
The implant pacing lead tined 3262 is a medical device designed to deliver electrical impulses to the heart to maintain an adequate heart rate. It is typically used in conjunction with a pacemaker. The tined design helps secure the lead within the heart tissue, ensuring stable positioning and effective pacing.
Clinical Applications
This device is commonly used in cardiac pacing procedures, particularly in patients with bradycardia or other arrhythmias requiring pacing support. It is utilized in hospital settings, often in cardiology departments, and is implanted by electrophysiologists or cardiologists. The patient population includes those with heart rhythm disorders who need long-term pacing solutions.
Indications for Use
The FDA indications suggest this device is intended for patients who require cardiac pacing due to conditions such as bradycardia. It is suitable for those who need consistent electrical stimulation to maintain heart rhythm.
Practical Considerations
The lead is typically available in various lengths to accommodate different patient anatomies. It is compatible with most pacemaker systems. Proper technique during implantation is crucial to ensure lead stability and function.
Frequently Asked Questions
What is the implant pacing lead tined 3262 used for?
It is used for cardiac pacing in patients who require electrical stimulation to maintain heart rhythm.
What specialties typically use this device?
Cardiologists and electrophysiologists typically use this device in cardiac pacing procedures.
What are the FDA-cleared indications?
The device is indicated for patients needing cardiac pacing due to conditions like bradycardia.
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.