510(k) Report

PMA · Approved

Approved

Ciba Corning Acs Psa Immunoassay

P920030PMAApproved Dec 8, 19982,356-day reviewClass II21 CFR 866.6010

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

Bayer Healthcare, LLC · LTJ Prostate-Specific Antigen (Psa) For Management Of Prostate Cancers

Approved on Dec 8, 1998 through premarket approval, which rests on the device’s own clinical evidence after a 2,356-day review. 2 later devices descend from it.

Decided
Dec 8, 1998
Review
2,356 days
Class
Class II
Product code
LTJ
Recalls
None

2 later devices descend from it, 1 citing it directly.

Descendants, by year cleared 1998: 1 descendant cleared2002: 1 descendant cleared1995200020052010201520202025
  1. This deviceP920030 Ciba Corning Acs Psa ImmunoassayBayer Healthcare, LLC · 1998
  2. Descendant · cites it directly · 1 of its ownK981592 Acs:Centaur AfpChiron Diagnostics Corp. · 1998
  3. Descendant · 2 generations on · 0 of its ownK020806 Acs:180 & Advia Centaur Afp ImmunoassayBayer Corp. · 2002

Most influential descendants

Showing 2 of 2 · See all
  • K981592Acs:Centaur AfpChiron Diagnostics Corp. · 1998 · cites it directly1descendant
  • K020806Acs:180 & Advia Centaur Afp ImmunoassayBayer Corp. · 2002 · 2 generations on0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)P920030Ciba Corning Acs Psa ImmunoassayBayer Healthcare, LLC1998—
+1K981592Acs:Centaur AfpChiron Diagnostics Corp.1998—
+2K020806Acs:180 & Advia Centaur Afp ImmunoassayBayer Corp.2002—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
199810
200210
FIG. 1 — Lineage of P920030, 1998–2002Source: 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 PMA database (decision fields and supplements), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.

Planning a device in LTJ? 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 LTJ device

  1. #1 K251630 Atellica IM Total PSA II (tPSAII)score 10.6 · 1 generation · no Class I recall
Get a 510(k) Report

Does it have a predicate?

PMA decisions do not claim a predicate device.

What descends from it? (2)

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

NumberDeviceApplicantDecidedDescendants
K981592Acs:Centaur AfpChiron Diagnostics Corp.19981

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, K981592 (Chiron Diagnostics Corp., 1998) has gone furthest, with 1 descendant of its own.

How does its category compare?

All LTJ devices

LTJ Prostate-Specific Antigen (Psa) For Management Of Prostate Cancers: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · LTJ

3in 2025

2013: 12016: 22017: 102018: 72019: 22020: 12021: 22023: 22024: 32025: 32026 (partial year): 3
2007high 10 (2017) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · LTJ

Too few LTJ 510(k)s in any year since 2007 to give a median.

Recalls per year · LTJ

1in 2025

2008: 32010: 22013: 12025: 1
2007high 3 (2008) · low 0 (2007)2026

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

Adverse event reports per year · LTJ

14in 2025

2007: 172008: 572009: 582010: 342011: 1092012: 1012013: 692014: 192015: 142016: 82017: 132018: 82019: 112020: 42021: 82022: 112023: 172024: 82025: 14
2007high 109 (2011) · low 4 (2020)2025

MAUDE reports naming product code LTJ, 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—017
20080—357
20090—058
20100—234
20110—0109
20120—0101
20131—169
20140—019
20150—014
20162—08
201710—013
20187—08
20192—011
20201—04
20212—08
20220—011
20232—017
20243—08
20253—114
20263—0—
Cite this page

510(k) Report. “P920030: Ciba Corning Acs Psa Immunoassay.” Lineage record from FDA PMA data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/P920030

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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