510(k) Report

510(k) · Cleared

Cleared

Sydney Ivf Sperm Medium, Sydney Ivf Sperm Gradient Kit, Sydney Ivf Spermient

K152782510(k) SpecialCleared Dec 21, 201587-day reviewClass II21 CFR 884.6180

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

William A. Cook Australia Pty., Ltd. · MQL Media, Reproductive

Cleared on Dec 21, 2015 as substantially equivalent to K002383 (Cook Ob/Gyn, 2000) after an 87-day review. Its family tree reaches back 1 generation to 2000. 4 later devices descend from it.

Decided
Dec 21, 2015
Review
87 days
Class
Class II
Product code
MQL
Recalls
None
Predicates
1

Its longest line of descent runs back 1 generation to K002383 (2000). 4 later devices descend from it, 1 citing it directly.

Descendants, by year cleared 2019: 1 descendant cleared2020: 1 descendant cleared2022: 1 descendant cleared2024: 1 descendant clearedK002383 · Cook Ivf Sperm Buffer, Cook Ivf Sperm Medium, and Cook Ivf Sperm Gradient Kit · Cook Ob/Gyn · 2000200020052010201520202025
Descendants, by generation 1 generation forward: 1 descendant2 generations forward: 2 descendants3 generations forward: 1 descendant K002383 · Cook Ivf Sperm Buffer, Cook Ivf Sperm Medium, and Cook Ivf Sperm Gradient Kit · Cook Ob/Gyn · 20000
  1. Root · 1 generation backK002383 Cook Ivf Sperm Buffer, Cook Ivf Sperm Medium, and Cook Ivf Sperm…Cook Ob/Gyn · 2000
  2. This deviceK152782 Sydney Ivf Sperm Medium, Sydney Ivf Sperm Gradient Kit, Sydney Ivf…William A. Cook Australia Pty., Ltd. · 2015
  3. Descendant · cites it directly · 3 of its ownK190199 SepaSperm Washing Solution, SepaSperm SolutionKitazato Corporation · 2019
  4. Descendant · 2 generations on · 1 of its ownK212410 VitaVitro Sperm Washing Medium, VitaVitro Sperm Gradient MediumShenzhen Vitavitro Biotech Co., Ltd. · 2022
  5. Descendant · 3 generations on · 0 of its ownK241095 ARTSMedia Semen Wash MediumArtsmedia Denmark Aps · 2024
  6. Descendant · 2 generations on · 0 of its ownK192644 GM501 SpermAir and GM501 SpermActiveHamilton Thorne Incorporated · 2020

Most influential descendants

Showing 4 of 4 · See all
  • K190199SepaSperm Washing Solution, SepaSperm SolutionKitazato Corporation · 2019 · cites it directly3descendants
  • K212410VitaVitro Sperm Washing Medium, VitaVitro Sperm Gradient MediumShenzhen Vitavitro Biotech Co., Ltd. · 2022 · 2 generations on1descendant
  • K241095ARTSMedia Semen Wash MediumArtsmedia Denmark Aps · 2024 · 3 generations on0descendants
  • K192644GM501 SpermAir and GM501 SpermActiveHamilton Thorne Incorporated · 2020 · 2 generations on0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−1K002383Cook Ivf Sperm Buffer, Cook Ivf Sperm Medium, and Cook Ivf Sperm Gradient KitCook Ob/Gyn2000—
0 (this device)K152782Sydney Ivf Sperm Medium, Sydney Ivf Sperm Gradient Kit, Sydney Ivf SpermientWilliam A. Cook Australia Pty., Ltd.2015—
+1K190199SepaSperm Washing Solution, SepaSperm SolutionKitazato Corporation2019—
+2K212410VitaVitro Sperm Washing Medium, VitaVitro Sperm Gradient MediumShenzhen Vitavitro Biotech Co., Ltd.2022—
+3K241095ARTSMedia Semen Wash MediumArtsmedia Denmark Aps2024—
+2K192644GM501 SpermAir and GM501 SpermActiveHamilton Thorne Incorporated2020—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201910
202010
202210
202410
FIG. 1 — Lineage of K152782, 2000–2024Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

Get the monthly Device Review Tracker

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 MQL? 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 MQL device

  1. #1 K251305 Ultra-Fast Vitri; Ultra-Fast Warmscore 14.4 · 6 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
Get a 510(k) Report

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
*K002383Cook Ivf Sperm Buffer, Cook Ivf Sperm Medium, and Cook Ivf Sperm Gradient Kit
Summary page 6
…latory Class: II Product Code: MQL - Media, Reproductive PREDICATE DEVICE: Cook IVF Sperm Buffer, Cook IVF Sperm Medium, and Cook IVF Sperm Gradient Kit (K002383), cleared September 13, 2000. DEVICE DESCRIPTION: The Sydney IVF Sperm Medium, Sydney IVF Sperm Gradient Kit and Sydney IVF Spe…
Cook Ob/Gyn2000—

What descends from it? (4)

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

NumberDeviceApplicantDecidedDescendants
K190199SepaSperm Washing Solution, SepaSperm SolutionKitazato Corporation20193

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, K190199 (Kitazato Corporation, 2019) has gone furthest, with 3 descendants of its own.

How does its category compare?

All MQL devices

MQL Media, Reproductive: FDA decisions, review times, recalls and adverse event reports over 20 years. 2015, this device’s year, is highlighted.

FDA decisions per year · MQL

9in 2025

2007: 32008: 122009: 22010: 62011: 12012: 52014: 52015: 72016: 122017: 102018: 42019: 62020: 82021: 12022: 32023: 52024: 122025: 92026 (partial year): 3
2007high 12 (2008) · low 0 (2013)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · MQL

225in 2025

2007: 212 days median2008: 151 days median2010: 235 days median2012: 253 days median2014: 142 days median2015: 87 days median2016: 170 days median2017: 113 days median2018: 94 days median2019: 170 days median2020: 257 days median2022: 316 days median2023: 199 days median2024: 195 days median2025: 225 days median2026 (partial year): 179 days median
2007high 316 (2022) · low 87 (2015)2026

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

Recalls per year · MQL

1in 2023

2012: 12020: 12021: 22022: 12023: 1
2007high 2 (2021) · low 0 (2007)2026

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

Adverse event reports per year · MQL

3in 2025

2012: 12013: 22014: 32016: 22023: 12024: 62025: 3
2007high 6 (2024) · low 0 (2007)2025

MAUDE reports naming product code MQL, 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
2007321200
20081215100
20092—00
2010623500
20111—00
2012525311
20130—02
2014514203
201578700
20161217002
20171011300
201849400
2019617000
2020825710
20211—20
2022331610
2023519911
20241219506
2025922503
202631790—

What is it indicated for?

Sydney IVF Sperm Medium is intended for use during in vitro fertilization procedures to process sperm.

Sydney IVF Sperm Gradient Kit is intended for use during in vitro fertilization procedures to separate motile sperm from seminal plasma.

Sydney IVF Spermient is intended for use during in vitro fertilization procedures to separate motile sperm from seminal plasma.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K152782: Sydney Ivf Sperm Medium, Sydney Ivf Sperm Gradient Kit, Sydney Ivf Spermient.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K152782

Report an extraction error

Tell us what is wrong; we check it against the FDA summary.

Are you the manufacturer?

Send a correction or an update to this page, for example a newer model or a public statement about a recall.

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