# K841547: Hemoclip Ligating Clips Med/SML

- Pathway: 510(k) (Traditional)
- Applicant: Edward Weck, Inc.
- Decided: Aug 14, 1984 after 120 days
- Product code: FZP (Clip, Implantable)
- Device class: 2
- Regulation: 21 CFR 878.4300
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
3 later devices descend from it; 2 cite it directly.
0 of 4 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
- K132658: Hemoclip Traditional Ligating Clips, Hemoclip Plus Ligating Clips, Horizon Ligting Clips (2013), 1 descendant of its own
- K192711: Dannik Titanium Ligation Clip (2019), 0 descendants of its own
- K091060: Vesocclude Ligating Clip (2009), 0 descendants of its own

Source page: https://510kreport.com/device/K841547
Methodology: https://510kreport.com/methodology