510(k) Report

510(k) · Cleared

Cleared

Iui Catheter, Model 9057

K052059510(k) AbbreviatedCleared Nov 22, 2005116-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

Inntec, Inc. · MQF Catheter, Assisted Reproduction

Cleared on Nov 22, 2005 as substantially equivalent to K921518 (Lifetek Medical, Inc., 1994) after a 116-day review. Its family tree reaches back 1 generation to 1994.

Decided
Nov 22, 2005
Review
116 days
Class
Class II
Product code
MQF
Recalls
None
Predicates
1

Its longest line of descent runs back 1 generation to K921518 (1994). No later device cites it as a predicate yet.

K921518 · Lifetek Iui Catheter · Lifetek Medical, Inc. · 19941990199520002005
K921518 · Lifetek Iui Catheter · Lifetek Medical, Inc. · 19940
  1. Root · 1 generation backK921518 Lifetek Iui CatheterLifetek Medical, Inc. · 1994
  2. This deviceK052059 Iui Catheter, Model 9057Inntec, Inc. · 2005
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−1K921518Lifetek Iui CatheterLifetek Medical, Inc.1994—
0 (this device)K052059Iui Catheter, Model 9057Inntec, Inc.2005—
FIG. 1 — Lineage of K052059, 1994–2005Source: FDA 510(k) summaries, read by 510(k) Report · 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 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. #1 K253354 Minvitro Embryo Transfer Catheters (ETCA23175…score 11.4 · 3 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.

TypeNumberDeviceApplicantDecidedRecalls
*K921518Lifetek Iui Catheter
Summary page 1
…510(k) Manufactur Product Class Trade Name er Code K921518 Lifetek MFD 11 [U1 Catheter Medical, Inc.…
Lifetek Medical, Inc.1994—

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.

What does this lineage say?

  • Its one ancestor has no recall.

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

2010: 12012: 22013: 12015: 22017: 62018: 52019: 22020: 22022: 12023: 12024: 12025: 12026 (partial year): 1
2007high 6 (2017) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · MQF

196in 2018

2017: 230 days median2018: 196 days median
2007high 230 (2017) · low 196 (2018)2026

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

Recalls per year · MQF

2in 2019

2007: 62019: 2
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

2007: 22010: 32014: 32015: 22016: 32017: 102018: 272019: 162020: 192021: 132022: 112023: 122024: 152025: 13
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
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
20070—62
20080—00
20090—00
20101—03
20110—00
20122—00
20131—00
20140—03
20152—02
20160—03
20176230010
20185196027
20192—216
20202—019
20210—013
20221—011
20231—012
20241—015
20251—013
20261—0—

What is it indicated for?

The InnTec, Inc. Intrauterine Insemination (IUI) Catheter is used for intrauterine insemination.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K052059: Iui Catheter, Model 9057.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K052059

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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