510(k) Report

510(k) · Cleared

Cleared

Disp. Teflon Connhctor

K771429510(k) TraditionalCleared Dec 22, 1977143-day reviewClass I21 CFR 876.5540

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

Quinton, Inc. · FJQ Connector, Shunt

Cleared on Dec 22, 1977 after a 143-day review. FDA has not posted a summary or statement for it, so its predicates are not known.

Decided
Dec 22, 1977
Review
143 days
Class
Class I
Product code
FJQ
Recalls
None
Predicates
0

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

FIG. 1 — Lineage of K771429Source: 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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  • Recall history across each candidate’s familyin the report
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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 FJQ devices

FJQ Connector, Shunt: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · FJQ

FDA has decided no FJQ device since 2007.

Median 510(k) review, days · FJQ

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

Recalls per year · FJQ

No recall names FJQ since 2007.

Adverse event reports per year · FJQ

No MAUDE report names FJQ 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—

More from Quinton, Inc.

164 FDA decisions under this applicant name. See the company

  • K032038Pyramis Ecg Management System Model Numbers, 92600 and 92601Quinton, Inc. · 2003
  • K021906Quinton Q-Cath, Model 000460Quinton, Inc. · 2002
  • K003576Q-Tel RMS (Rehabilitation Management System), Model 000503Quinton, Inc. · 20011 recall
  • K001492Quinton Q-Stress, Model 000483Quinton, Inc. · 2000
  • K992908Q-Tel Telemetry System V. 6.0 (ST)Quinton, Inc. · 2000

Recent decisions in FJQ

The FJQ category page

  • K893679Shunt ConnectorsAkcess Medical Products, Inc. · 1989
  • K771422Patient by-PassQuinton, Inc. · 1978

https://510kreport.com/device/K771429 · printed Nov 4, 2026

Cite this page

510(k) Report. “K771429: Disp. Teflon Connhctor.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K771429

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