510(k) Report

510(k) · Cleared

Cleared

Reagent System

K760821510(k) TraditionalCleared Oct 21, 19768-day reviewClass I21 CFR 862.1040

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

Sigma Chemical Co. · CJT Hydrazone Colorimetry, Aldolase

Cleared on Oct 21, 1976 after an 8-day review. FDA has not posted a summary or statement for it, so its predicates are not known.

Decided
Oct 21, 1976
Review
8 days
Class
Class I
Product code
CJT
Recalls
None
Predicates
0

FDA has not posted a summary or statement for it, so its predicates are not known.

FIG. 1 — Lineage of K760821Source: FDA 510(k) database · 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.

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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?

No later submission names this one as a predicate yet.

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.

How does its category compare?

All CJT devices

CJT Hydrazone Colorimetry, Aldolase: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · CJT

FDA has decided no CJT device since 2007.

Median 510(k) review, days · CJT

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

Recalls per year · CJT

No recall names CJT since 2007.

Adverse event reports per year · CJT

No MAUDE report names CJT since 2007.

View these four charts as a table
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
20070—00
20080—00
20090—00
20100—00
20110—00
20120—00
20130—00
20140—00
20150—00
20160—00
20170—00
20180—00
20190—00
20200—00
20210—00
20220—00
20230—00
20240—00
20250—00
20260—0—
Cite this page

510(k) Report. “K760821: Reagent System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K760821

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