# K131614: Reprocessed Closurefast Radiofrequency Catheter 60CM, Reprocessed Closurefast Radiofrequency Catheter 100CM

- Pathway: 510(k) (Traditional)
- Applicant: Covidien
- Decided: Aug 29, 2013 after 87 days
- Product code: NUJ (Electrosurgical, Cutting & Coagulation Accessories, Laparoscopic & Endoscopic, Reprocessed)
- Device class: 2
- Regulation: 21 CFR 878.4400
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The summary cites one number, which could not be confirmed as its predicate (listed below).

## Cited in the summary but kept off the family tree
- K0611373: ClosureFast RF Catheter. Number could not be read Summary page 2.

## Indications for use
The Reprocessed ClosureFast RF Catheter is intended for endovascular coagulation of blood vessels in patients with superficial vein reflux.

Source page: https://510kreport.com/device/K131614
Methodology: https://510kreport.com/methodology