510(k) · Cleared
ClearedAcon HCG One Step Urine/Serum Pregnancy Test
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Acon Laboratories Co. · JHI Visual, Pregnancy Hcg, Prescription Use
Cleared on Apr 16, 1998 as substantially equivalent to K903219 (Abbott Laboratories, 1990) after a 50-day review. Its family tree reaches back 1 generation to 1990. 1 later device descends from it.
- Decided
- Apr 16, 1998
- Review
- 50 days
- Class
- Class II
- Product code
- JHI
- Recalls
- None
- Predicates
- 1
Its longest line of descent runs back 1 generation to K903219 (1990). 1 later device descends from it, 1 citing it directly.
- Root · 1 generation backK903219 Abbott Testpack Plus TM HCG-ComboAbbott Laboratories · 1990 · Recalled
- This deviceK980736 Acon HCG One Step Urine/Serum Pregnancy TestAcon Laboratories Co. · 1998
- Descendant · cites it directly · 0 of its ownK072500 One Step HCG Urine/Serum TestGuangzhou Wondfo Biotech Co., Ltd. · 2009
Most influential descendants
Showing 1 of 1 · See all- K072500One Step HCG Urine/Serum TestGuangzhou Wondfo Biotech Co., Ltd. · 2009 · cites it directly0descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −1 | K903219 | Abbott Testpack Plus TM HCG-Combo | Abbott Laboratories | 1990 | 1 |
| 0 (this device) | K980736 | Acon HCG One Step Urine/Serum Pregnancy Test | Acon Laboratories Co. | 1998 | — |
| +1 | K072500 | One Step HCG Urine/Serum Test | Guangzhou Wondfo Biotech Co., Ltd. | 2009 | — |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2009 | 1 | 0 |
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 JHI? 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 JHI device
- #1 K262299 Instant-View® hCG Combo II Cassette Testscore 12.7 · 3 generations · no Class I recall
- #2 Held for the reportin the report
- #3 Held for the reportin the 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.
| Type | Number | Device | Decided |
|---|---|---|---|
| * | K903219 | Abbott Testpack Plus TM HCG-ComboSummary page 2…lly Marketed Device The ACON® hCG Urine/Serum One Step Pregnancy Test has been determined to be substantially equivalent to the TestPack®Plus™ hCG Combo pregnancy test (K903219) currently in commercial distribution by Abbott. D. Device Description The ACON hCG Urine/Serum One Step Pregnancy Test is a ra… | 1990 |
What descends from it? (1)
1 later device cites it directly; ranked here by how many devices descend from each in turn.
| Number | Device | Decided | Descendants |
|---|---|---|---|
| K072500 | One Step HCG Urine/Serum Test | 2009 | 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 a recall.
- Of its descendants, K072500 (Guangzhou Wondfo Biotech Co., Ltd., 2009) has gone furthest, with 0 descendants of its own.
How does its category compare?
All JHI devicesJHI Visual, Pregnancy Hcg, Prescription Use: FDA decisions, review times, recalls and adverse event reports over 20 years.
FDA decisions per year · JHI
1in 2024
2026 to Oct 25, outlined.
Median 510(k) review, days · JHI
101in 2007
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · JHI
1in 2024
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · JHI
265in 2025
MAUDE reports naming product code JHI, 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 | 4 | 101 | 6 | 245 |
| 2008 | 0 | — | 8 | 29 |
| 2009 | 0 | — | 1 | 106 |
| 2010 | 1 | — | 2 | 143 |
| 2011 | 0 | — | 1 | 138 |
| 2012 | 2 | — | 0 | 219 |
| 2013 | 2 | — | 0 | 185 |
| 2014 | 2 | — | 0 | 112 |
| 2015 | 0 | — | 0 | 134 |
| 2016 | 1 | — | 0 | 143 |
| 2017 | 1 | — | 0 | 113 |
| 2018 | 1 | — | 0 | 132 |
| 2019 | 0 | — | 0 | 571 |
| 2020 | 0 | — | 0 | 114 |
| 2021 | 0 | — | 0 | 158 |
| 2022 | 1 | — | 0 | 126 |
| 2023 | 0 | — | 6 | 147 |
| 2024 | 1 | — | 1 | 256 |
| 2025 | 0 | — | 0 | 265 |
| 2026 | 1 | — | 4 | — |
What is it indicated for?
The ACON hCG Urine/Serum One Step Pregnancy Test is a rapid qualitative chromatographic immunoassay for the detection of human chorionic gonadotropin in urine or serum.
The ACON hCG Urine/Serum One Step Pregnancy Test is indicated for use as an aid in the early detection of pragnancy. This device is intended to be used in the clinical laboratory and/or physician's office.
Indications for use read by OCR from a scanned FDA summary, so letters may be misread. Check the PDF before quoting it.
https://510kreport.com/device/K980736 · printed Nov 4, 2026
Cite this page
510(k) Report. “K980736: Acon HCG One Step Urine/Serum Pregnancy Test.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K980736
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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