510(k) · Cleared

Cleared

Coopersurgical Trial Transfer Catheter

K023384510(k) TraditionalCleared Dec 13, 200266-day reviewClass II21 CFR 884.6110

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

Cooper Surgical · MQF Catheter, Assisted Reproduction

Cleared on Dec 13, 2002 as substantially equivalent to K990348 (CooperSurgical, Inc., 1999) after a 66-day review. Its family tree reaches back 1 generation to 1999. 1 later device descends from it.

Decided: Dec 13, 2002
Review: 66 days
Class: Class II
Product code: MQF
Recalls: None
Predicates: 1

Its longest line of descent runs back 1 generation to K990348 (1999). 1 later device descends from it, 1 citing it directly.

By dateBy generation

Root · 1 generation backK990348 Wallace Trial Transfer Catheter, Model TT 1816NCooperSurgical, Inc. · 1999
This deviceK023384 Coopersurgical Trial Transfer CatheterCooper Surgical · 2002
Descendant · cites it directly · 0 of its ownK053208 Clear Vision Embryo Transfer Catheter Set, Model B100000 - B 100007…Swemed Lab International AB · 2006

Most influential descendants

Showing 1 of 1 · See all

K053208Clear Vision Embryo Transfer Catheter Set, Model B100000 - B 100007; Clear Vision Trial…Swemed Lab International AB · 2006 · cites it directly0descendants

View FIG. 1 as a table

Line of descent and top descendants

Generation	Number	Device	Applicant	Decided	Recalls
−1	K990348	Wallace Trial Transfer Catheter, Model TT 1816N	CooperSurgical, Inc.	1999	—
0 (this device)	K023384	Coopersurgical Trial Transfer Catheter	Cooper Surgical	2002	—
+1	K053208	Clear Vision Embryo Transfer Catheter Set, Model B100000 - B 100007; Clear…	Swemed Lab International AB	2006	—

Descendants by year cleared

Year cleared	Devices	With a Class I recall
2006	1	0

FIG. 1 — Lineage of K023384, 1999–2006Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

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 MQF? 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 MQF device

#1 K253354 Minvitro Embryo Transfer Catheters (ETCA23175…score 11.4 · 3 generations · no Class I recall
#2 Held for the reportin the report
#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.

Type	Number	Device	Applicant	Decided	Recalls
*	K990348	Wallace Trial Transfer Catheter, Model TT 1816N	CooperSurgical, Inc.	1999	—

Also cleared against K990348: 2 other devices →

What descends from it? (1)

1 later device cites it directly; ranked here by how many devices descend from each in turn.

Number	Device	Applicant	Decided	Descendants
K053208	Clear Vision Embryo Transfer Catheter Set, Model B100000 - B 100007; Clear Vision Trial…	Swemed Lab International AB	2006	0

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.

What does this lineage say?

Its one ancestor has no recall.
Of its descendants, K053208 (Swemed Lab International AB, 2006) has gone furthest, with 0 descendants of its own.
2 other devices also cite its predicate K990348.

How does its category compare?

All MQF devices

MQF Catheter, Assisted Reproduction: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · MQF

1in 2025

2007high 6 (2017) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · MQF

196in 2018

2007high 230 (2017) · low 196 (2018)2026

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

Recalls per year · MQF

2in 2019

2007high 6 (2007) · low 0 (2008)2026

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

Adverse event reports per year · MQF

13in 2025

2007high 27 (2018) · low 0 (2008)2025

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

View these four charts as a table

Year	Decisions	Median 510(k) review, days	Recalls (Class I)	MAUDE reports
2007	0	—	6	2
2008	0	—	0	0
2009	0	—	0	0
2010	1	—	0	3
2011	0	—	0	0
2012	2	—	0	0
2013	1	—	0	0
2014	0	—	0	3
2015	2	—	0	2
2016	0	—	0	3
2017	6	230	0	10
2018	5	196	0	27
2019	2	—	2	16
2020	2	—	0	19
2021	0	—	0	13
2022	1	—	0	11
2023	1	—	0	12
2024	1	—	0	15
2025	1	—	0	13
2026	1	—	0	—

What is it indicated for?

The sterile single-use device is intended to assess advancement through the cervical canal and positioning of the

uterus.

Indications for use as stated in the FDA summary.

https://510kreport.com/device/K023384 · printed Nov 4, 2026

Cite this page

510(k) Report. “K023384: Coopersurgical Trial Transfer Catheter.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K023384

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Record history

FDA decision record loaded May 2, 2026
Summary read Oct 13, 2026 (extraction version 9eaa42aa01ed)
Lineage and recalls computed Nov 3, 2026
Page last updated Nov 3, 2026