Afterloading Catheter Set

K811279510(k) TraditionalCleared Aug 18, 1981102-day review

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

Cleared on Aug 18, 1981 after a 102-day review. FDA has not posted a summary or statement for it, so its predicates are not known. 2 later devices descend from it.

Decided: Aug 18, 1981
Review: 102 days
Recalls: None
Predicates: 0

2 later devices descend from it, 1 citing it directly.

This deviceK811279 Afterloading Catheter SetMick Radio-Nuclear Instruments, Inc. · 1981
Descendant · cites it directly · 1 of its ownK051423 Mick HDR Interstitial Implant AccessoriesMick Radio-Nuclear Instruments, Inc. · 2005
Descendant · 2 generations on · 0 of its ownK130757 Kobold Secure Lock Transfer Guide Tube Set; Kobold Luer Transfer…Spencer Fillmore · 2014

Most influential descendants

Showing 2 of 2 · See all

K051423Mick HDR Interstitial Implant AccessoriesMick Radio-Nuclear Instruments, Inc. · 2005 · cites it directly1descendant
K130757Kobold Secure Lock Transfer Guide Tube Set; Kobold Luer Transfer Guide Tube SetSpencer Fillmore · 2014 · 2 generations on0descendants

View FIG. 1 as a table

Line of descent and top descendants

Generation	Number	Device	Applicant	Decided	Recalls
0 (this device)	K811279	Afterloading Catheter Set	Mick Radio-Nuclear Instruments, Inc.	1981	—
+1	K051423	Mick HDR Interstitial Implant Accessories	Mick Radio-Nuclear Instruments, Inc.	2005	—
+2	K130757	Kobold Secure Lock Transfer Guide Tube Set; Kobold Luer Transfer Guide Tube Set	Spencer Fillmore	2014	—

Descendants by year cleared

Year cleared	Devices	With a Class I recall
2005	1	0
2014	1	0

FIG. 1 — Lineage of K811279, 1981–2014Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

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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Candidate predicates for a device like this, rankedin the report
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? (2)

1 later device cites it directly; ranked here by how many devices descend from each in turn.

Number	Device	Applicant	Decided	Descendants
K051423	Mick HDR Interstitial Implant Accessories	Mick Radio-Nuclear Instruments, Inc.	2005	1

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, K051423 (Mick Radio-Nuclear Instruments, Inc., 2005) has gone furthest, with 1 descendant of its own.

https://510kreport.com/device/K811279 · printed Nov 6, 2026

Cite this page

510(k) Report. “K811279: Afterloading Catheter Set.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K811279

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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