510(k) Report

510(k) · Cleared

Cleared

Reprocessed Closurefast Radiofrequency Catheter 60CM, Reprocessed Closurefast Radiofrequency Catheter 100CM

K131614510(k) TraditionalCleared Aug 29, 201387-day reviewClass II21 CFR 878.4400

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly, last Nov 3, 2026

Covidien · NUJ Electrosurgical, Cutting & Coagulation Accessories, Laparoscopic & Endoscopic, Reprocessed

Cleared on Aug 29, 2013 after an 87-day review. The summary cites one number, which could not be confirmed as its predicate (see the table below).

Decided
Aug 29, 2013
Review
87 days
Class
Class II
Product code
NUJ
Recalls
None
Predicates
1

The summary cites one number, which could not be confirmed as its predicate (see the table below).

FIG. 1 — Lineage of K131614Source: FDA 510(k) database · How lineage is built

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Notable FDA decisions, review times and new Class I recalls. See an issue.

Sources: FDA 510(k) database (decision fields), the FDA summary (predicates and indications), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.

Planning a device in NUJ? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.

Top candidate predicates for a new NUJ device

  1. #1 K220411 Reprocessed LigaSure Curved, Small Jaw, Open…score 8.4 · 8 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
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What was it cleared against? (1)

Devices the submitter claimed this one is substantially equivalent to (*), and reference devices cited for a specific test or feature (†), as written in the FDA summary; numbers the summary cites that cannot be its predicate are marked – and kept off the family tree.

TypeNumberDeviceApplicantDecidedRecalls
Kept off the family treeK0611373ClosureFast RF Catheter
Number could not be read
Summary page 2
…des that the Reprocessed ClosureFast RF Catheter is safe, effective, and substantially equivalent to the predicate device, ClosurelFast RIF Catheters K0611373, as described in this premnarket notification submission. 5/31/13…

What descends from it?

No later submission names this one as a predicate yet.

Has anything in its family been recalled? (0 Class I)

No FDA recall names this device.

No ancestor or descendant has a Class I recall.

How does its category compare?

All NUJ devices

NUJ Electrosurgical, Cutting & Coagulation Accessories, Laparoscopic & Endoscopic, Reprocessed: FDA decisions, review times, recalls and adverse event reports over 20 years. 2013, this device’s year, is highlighted.

FDA decisions per year · NUJ

1in 2024

2008: 12010: 12011: 22012: 22013: 22014: 12015: 22016: 52017: 32018: 72019: 12022: 22023: 12024: 1
2007high 7 (2018) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · NUJ

88in 2018

2016: 155 days median2017: 49 days median2018: 88 days median
2007high 155 (2016) · low 49 (2017)2026

Receipt to decision; years with fewer than 3 clearances left blank.

Recalls per year · NUJ

11in 2025

2008: 22023: 32025: 11
2007high 11 (2025) · low 0 (2007)2026

Class I (0 since 2007) Class II/III not classified

Adverse event reports per year · NUJ

38in 2025

2007: 42008: 42009: 12010: 92011: 22012: 392013: 1612014: 742015: 252016: 522017: 512018: 142019: 202020: 592021: 472022: 312023: 272024: 922025: 38
2007high 161 (2013) · low 1 (2009)2025

MAUDE reports naming product code NUJ, not matched to any one device; reports are not rates.

View these four charts as a table
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
20070—04
20081—24
20090—01
20101—09
20112—02
20122—039
20132—0161
20141—074
20152—025
20165155052
2017349051
2018788014
20191—020
20200—059
20210—047
20222—031
20231—327
20241—092
20250—1138
20260—0—

What is it indicated for?

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

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K131614: Reprocessed Closurefast Radiofrequency Catheter 60CM, Reprocessed Closurefast Radiofrequency Catheter 100CM.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K131614

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Record history
  • FDA decision record loaded May 2, 2026
  • Summary read Oct 13, 2026 (extraction version 9eaa42aa01ed)
  • Page last updated Nov 3, 2026