510(k) Report

FDA product code · Cardiovascular

Catheter Introducer Kit

OFCClass II21 CFR 870.13401 decision since 20104 recalls

1 FDA decision since 2010. 4 recalls name this code, 1 of them Class I.

This product code has been established in accordance with the may 20, 1997, guidance entitled, convenience kits interim regulatory guidance, found at www.Fda.Gov/cdrh/ode/convkit.Html. This type of convenience kit, as listed in the guidance above, is under enforcement discretion, and does not require a premarket notification (510(k)) to market if it meets all criteria in the guidance.

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

FIG. A — Illustration, cardiovascular panel

Twenty years of OFC at a glance: how often FDA decides these devices, how long 510(k) reviews take, how often they are recalled, and how many adverse event reports name the code.

FDA decisions per year · OFC

1in 2010

2010: 1
2007high 1 (2010) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · OFC

Too few OFC 510(k)s in any year since 2007 to give a median.

Recalls per year · OFC

3so far in 2026, the most since 2007

2020: 12026 (partial year): 3, 1 Class I
2007high 3 (2026) · low 0 (2007)2026

Class I (1 since 2007) Class II/III not classified

Adverse event reports per year · OFC

3in 2025

2016: 22017: 22018: 12019: 52020: 12021: 42022: 42023: 82024: 82025: 3
2007high 8 (2023) · low 0 (2007)2025

MAUDE reports naming product code OFC, 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—00
20080—00
20090—00
20101—00
20110—00
20120—00
20130—00
20140—00
20150—00
20160—02
20170—02
20180—01
20190—05
20200—11
20210—04
20220—04
20230—08
20240—08
20250—03
20260—3 (1)—
FIG. 1 — OFC by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports, MAUDE · Data through Oct 25, 2026

Planning a device in OFC? A 510(k) Report ranks candidate predicates in this code by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Related product codes

Other codes under 21 CFR 870.1340.