510(k) Report

510(k) · Cleared

Cleared

Cobas Reagent for a-Amylase

K801295510(k) TraditionalCleared Jul 8, 198036-day reviewClass II21 CFR 862.1070

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

Roche Analytical Instruments, Inc. · JFJ Catalytic Methods, Amylase

Cleared on Jul 8, 1980 after a 36-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 8, 1980
Review
36 days
Class
Class II
Product code
JFJ
Recalls
None
Predicates
0

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

Descendants, by year cleared 2006: 1 descendant cleared19801990200020102020
  1. This deviceK801295 Cobas Reagent for a-AmylaseRoche Analytical Instruments, Inc. · 1980
  2. Descendant · cites it directly · 0 of its ownK062180 Abx Pentra Amylase CP; Multical; N Control; P Control; Clean-Chem…Horiba Abx · 2006

Most influential descendants

Showing 1 of 1 · See all
  • K062180Abx Pentra Amylase CP; Multical; N Control; P Control; Clean-Chem CP; Clean-Chem 99 CPHoriba Abx · 2006 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K801295Cobas Reagent for a-AmylaseRoche Analytical Instruments, Inc.1980—
+1K062180Abx Pentra Amylase CP; Multical; N Control; P Control; Clean-Chem CP…Horiba Abx2006—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
200610
FIG. 1 — Lineage of K801295, 1980–2006Source: 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 JFJ? 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 JFJ device

  1. #1 K210633 Amylase2score 3.7 · 2 generations · no Class I recall
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
K062180Abx Pentra Amylase CP; Multical; N Control; P Control; Clean-Chem CP; Clean-Chem 99 CPHoriba Abx20060

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, K062180 (Horiba Abx, 2006) has gone furthest, with 0 descendants of its own.

How does its category compare?

All JFJ devices

JFJ Catalytic Methods, Amylase: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · JFJ

1in 2022

2007: 12008: 12009: 12012: 12013: 12019: 22022: 1
2007high 2 (2019) · low 0 (2010)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · JFJ

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

Recalls per year · JFJ

1in 2007

2007: 1
2007high 1 (2007) · low 0 (2008)2026

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

Adverse event reports per year · JFJ

1in 2025

2010: 12011: 22012: 12018: 22020: 12022: 12024: 12025: 1
2007high 2 (2011) · low 0 (2007)2025

MAUDE reports naming product code JFJ, 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
20071—10
20081—00
20091—00
20100—01
20110—02
20121—01
20131—00
20140—00
20150—00
20160—00
20170—00
20180—02
20192—00
20200—01
20210—00
20221—01
20230—00
20240—01
20250—01
20260—0—
Cite this page

510(k) Report. “K801295: Cobas Reagent for a-Amylase.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K801295

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