510(k) Report

PMA · Approved

Approved

AB -Havk

P890019PMAApproved Jul 13, 1990485-day reviewClass II21 CFR 866.3310

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

Diasorin · LOL Hepatitis A Test (Antibody And Igm Antibody)

Approved on Jul 13, 1990 through premarket approval, which rests on the device’s own clinical evidence after a 485-day review. 3 later devices descend from it.

Decided
Jul 13, 1990
Review
485 days
Class
Class II
Product code
LOL
Recalls
None

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

Descendants, by year cleared 2008: 1 descendant cleared2007: 1 descendant cleared2009: 1 descendant cleared1990200020102020
  1. This deviceP890019 AB -HavkDiasorin · 1990
  2. Descendant · cites it directly · 1 of its ownK063318 Monolisa Anti-Hav EiaBio-Rad Laboratories · 2007
  3. Descendant · 2 generations on · 0 of its ownK092355 Monolisa Anti-Hav EiaBio-Rad Laboratories, Inc. · 2009
  4. Descendant · cites it directly · 0 of its ownK082049 Liaison Anti-Hav Assay, Liaison Control Anti-HavDiaSorin, Inc. · 2008

Most influential descendants

Showing 3 of 3 · See all
  • K063318Monolisa Anti-Hav EiaBio-Rad Laboratories · 2007 · cites it directly1descendant
  • K092355Monolisa Anti-Hav EiaBio-Rad Laboratories, Inc. · 2009 · 2 generations on0descendants
  • K082049Liaison Anti-Hav Assay, Liaison Control Anti-HavDiaSorin, Inc. · 2008 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)P890019AB -HavkDiasorin1990—
+1K063318Monolisa Anti-Hav EiaBio-Rad Laboratories2007—
+2K092355Monolisa Anti-Hav EiaBio-Rad Laboratories, Inc.2009—
+1K082049Liaison Anti-Hav Assay, Liaison Control Anti-HavDiaSorin, Inc.2008—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
200710
200810
200910
FIG. 1 — Lineage of P890019, 1990–2009Source: 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 LOL? 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 LOL device

  1. #1 K251995 Access anti-HAV IgMscore 13.7 · 1 generation · 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

Does it have a predicate?

PMA decisions do not claim a predicate device.

What descends from it? (3)

2 later devices cite it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K063318Monolisa Anti-Hav EiaBio-Rad Laboratories20071
K082049Liaison Anti-Hav Assay, Liaison Control Anti-HavDiaSorin, Inc.20080

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, K063318 (Bio-Rad Laboratories, 2007) has gone furthest, with 1 descendant of its own.

How does its category compare?

All LOL devices

LOL Hepatitis A Test (Antibody And Igm Antibody): FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · LOL

1in 2025

2007: 32008: 32009: 22010: 22011: 12012: 12014: 22016: 22019: 12020: 12021: 12022: 12023: 12025: 12026 (partial year): 2
2007high 3 (2007) · low 0 (2013)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · LOL

108in 2008

2007: 182 days median2008: 108 days median
2007high 182 (2007) · low 108 (2008)2026

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

Recalls per year · LOL

2in 2019

2007: 22008: 12009: 12011: 12018: 12019: 2
2007high 2 (2007) · low 0 (2010)2026

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

Adverse event reports per year · LOL

19in 2025

2007: 22008: 132009: 242010: 532011: 3532012: 422013: 492014: 192015: 292016: 362017: 262018: 612019: 512020: 1042021: 122022: 172023: 362024: 212025: 19
2007high 353 (2011) · low 2 (2007)2025

MAUDE reports naming product code LOL, 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
2007318222
20083108113
20092—124
20102—053
20111—1353
20121—042
20130—049
20142—019
20150—029
20162—036
20170—026
20180—161
20191—251
20201—0104
20211—012
20221—017
20231—036
20240—021
20251—019
20262—0—
Cite this page

510(k) Report. “P890019: AB -Havk.” Lineage record from FDA PMA data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/P890019

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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