# K890341: Mick 200-TP and Mick TP Needle

- Pathway: 510(k) (Traditional)
- Applicant: Mick Radio-Nuclear Instruments, Inc.
- Decided: Mar 14, 1989 after 50 days
- Product code: IWJ (System, Applicator, Radionuclide, Manual)
- Device class: 1
- Regulation: 21 CFR 892.5650
- Recalls of this device: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
7 later devices descend from it; 4 cite it directly.
0 of 8 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K993400: HDR Contour TP Template and Implant Accessories (2000), 2 descendants of its own
- K051423: Mick HDR Interstitial Implant Accessories (2005), 1 descendant of its own
- K150979: CT/MR Compatible M.A.C. Interstitial GYN Template (2016), 0 descendants of its own
- K130757: Kobold Secure Lock Transfer Guide Tube Set; Kobold Luer Transfer Guide Tube Set (2014), 0 descendants of its own
- K072296: Poiint of Care Stranding System, Mode 1004-00 (2007), 0 descendants of its own

## Recalls of this device
- Mar 30, 2005 · Not classified · Z-0857-05: Some of the Mick TP Prostate Seeding Needles do not fit properly into the Mick 200-TPV Applicator. Firm received one complaint during use of the Mick 200 TPV Applicator.

Source page: https://510kreport.com/device/K890341
Methodology: https://510kreport.com/methodology