510(k) Report

510(k) · Cleared

Cleared

IL Test Lipase

K952647510(k) TraditionalCleared Jul 20, 199541-day reviewClass I21 CFR 862.1465

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

Instrumentation Laboratory CO · CHI Lipase-Esterase, Enzymatic, Photometric, Lipase

Cleared on Jul 20, 1995 after a 41-day review. FDA has not posted a summary or statement for it, so its predicates are not known. 1 later device descends from it.

Decided
Jul 20, 1995
Review
41 days
Class
Class I
Product code
CHI
Recalls
None
Predicates
0

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

Descendants, by year cleared 1998: 1 descendant cleared1995200020052010201520202025
  1. This deviceK952647 IL Test LipaseInstrumentation Laboratory CO · 1995
  2. Descendant · cites it directly · 0 of its ownK980757 Ilab 600 Clinical Chemistry SystemInstrumentation Laboratory CO · 1998

Most influential descendants

Showing 1 of 1 · See all
  • K980757Ilab 600 Clinical Chemistry SystemInstrumentation Laboratory CO · 1998 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K952647IL Test LipaseInstrumentation Laboratory CO1995—
+1K980757Ilab 600 Clinical Chemistry SystemInstrumentation Laboratory CO1998—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
199810
FIG. 1 — Lineage of K952647, 1995–1998Source: 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), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.

Planning a device in CHI? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.

  • Candidate predicates for a device like this, rankedin the report
  • Recall history across each candidate’s familyin the report
Get a 510(k) Report

What was it cleared against?

FDA has not posted a summary or statement for it, 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
K980757Ilab 600 Clinical Chemistry SystemInstrumentation Laboratory CO19980

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, K980757 (Instrumentation Laboratory CO, 1998) has gone furthest, with 0 descendants of its own.

How does its category compare?

All CHI devices

CHI Lipase-Esterase, Enzymatic, Photometric, Lipase: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · CHI

FDA has decided no CHI device since 2007.

Median 510(k) review, days · CHI

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

Recalls per year · CHI

1in 2023

2007: 12008: 42010: 12013: 12014: 12018: 32023: 1
2007high 4 (2008) · low 0 (2009)2026

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

Adverse event reports per year · CHI

11in 2025

2008: 12010: 22011: 42012: 12014: 12015: 52016: 32017: 42018: 62019: 22020: 322021: 22022: 42023: 42024: 62025: 11
2007high 32 (2020) · low 0 (2007)2025

MAUDE reports naming product code CHI, 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—10
20080—41
20090—00
20100—12
20110—04
20120—01
20130—10
20140—11
20150—05
20160—03
20170—04
20180—36
20190—02
20200—032
20210—02
20220—04
20230—14
20240—06
20250—011
20260—0—
Cite this page

510(k) Report. “K952647: IL Test Lipase.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K952647

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
  • Lineage and recalls computed Nov 3, 2026
  • Page last updated Nov 3, 2026