510(k) Report

510(k) · Cleared

Cleared

HCG Stat-Pak

K923925510(k) TraditionalCleared Dec 24, 1992141-day reviewClass II21 CFR 862.1155

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

Chembio Diagnostic Systems, Inc. · JHI Visual, Pregnancy Hcg, Prescription Use

Cleared on Dec 24, 1992 after a 141-day review. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known. 1 later device descends from it.

Decided
Dec 24, 1992
Review
141 days
Class
Class II
Product code
JHI
Recalls
None
Predicates
0

1 later device descends from it, 1 citing it directly.

Descendants, by year cleared 1996: 1 descendant cleared1990200020102020
  1. This deviceK923925 HCG Stat-PakChembio Diagnostic Systems, Inc. · 1992
  2. Descendant · cites it directly · 0 of its ownK961965 Sure Check Pregnancy TestChembio Diagnostic Systems, Inc. · 1996 · Recalled

Most influential descendants

Showing 1 of 1 · See all
  • K961965Sure Check Pregnancy TestChembio Diagnostic Systems, Inc. · 1996 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K923925HCG Stat-PakChembio Diagnostic Systems, Inc.1992—
+1K961965Sure Check Pregnancy TestChembio Diagnostic Systems, Inc.19961

Descendants by year cleared

Year clearedDevicesWith a Class I recall
199610
FIG. 1 — Lineage of K923925, 1992–1996Source: 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), 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. #1 K262299 Instant-View® hCG Combo II Cassette Testscore 12.7 · 3 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?

FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

What descends from it? (1)

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

NumberDeviceApplicantDecidedDescendants
K961965Sure Check Pregnancy TestChembio Diagnostic Systems, Inc.19960

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?

  • Of its descendants, K961965 (Chembio Diagnostic Systems, Inc., 1996) has gone furthest, with 0 descendants of its own.

How does its category compare?

All JHI devices

JHI Visual, Pregnancy Hcg, Prescription Use: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · JHI

1in 2024

2007: 42010: 12012: 22013: 22014: 22016: 12017: 12018: 12022: 12024: 12026 (partial year): 1
2007high 4 (2007) · low 0 (2008)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · JHI

101in 2007

2007: 101 days median
2007high 101 (2007)2026

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

Recalls per year · JHI

1in 2024

2007: 62008: 82009: 12010: 22011: 12023: 62024: 12026 (partial year): 4
2007high 8 (2008) · low 0 (2012)2026

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

Adverse event reports per year · JHI

265in 2025

2007: 2452008: 292009: 1062010: 1432011: 1382012: 2192013: 1852014: 1122015: 1342016: 1432017: 1132018: 1322019: 5712020: 1142021: 1582022: 1262023: 1472024: 2562025: 265
2007high 571 (2019) · low 29 (2008)2025

MAUDE reports naming product code JHI, 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
200741016245
20080—829
20090—1106
20101—2143
20110—1138
20122—0219
20132—0185
20142—0112
20150—0134
20161—0143
20171—0113
20181—0132
20190—0571
20200—0114
20210—0158
20221—0126
20230—6147
20241—1256
20250—0265
20261—4—
Cite this page

510(k) Report. “K923925: HCG Stat-Pak.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K923925

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Record history
  • FDA decision record loaded May 2, 2026
  • Lineage and recalls computed Nov 3, 2026
  • Page last updated Nov 3, 2026