# K895705: Shamrock Safety Blood Collection Set

- Pathway: 510(k) (Traditional)
- Applicant: Ryan Medical, Inc.
- Decided: Oct 10, 1989 after 29 days
- Product code: FMI (Needle, Hypodermic, Single Lumen)
- Device class: 2
- Regulation: 21 CFR 880.5570
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
15 later devices descend from it; 1 cites it directly.
0 of 16 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
- K072783: Saf-T Closed Blood Collection System with Saf-Holder Device, Model 99200, Saf-T Closed Blood Collection System with (2007), 14 descendants of its own
- K081229: Saf-T Closed Blood Collection System with Saf-Holder Device, with 21G, 23G, 25G Saf-T Wing (2008), 13 descendants of its own
- K142946: TIVA (2015), 8 descendants of its own
- K152924: TIVA¿ (2016), 7 descendants of its own
- K163508: PIVO (2017), 6 descendants of its own

Source page: https://510kreport.com/device/K895705
Methodology: https://510kreport.com/methodology
