# K182944: Dr. Amplatz Micro Plug

- Pathway: 510(k) (Traditional)
- Applicant: Ka Medical, LLC
- Decided: Apr 17, 2019 after 176 days
- Product code: KRD (Device, Vascular, For Promoting Embolization)
- Device class: 2
- Regulation: 21 CFR 870.3300
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
2 later devices descend from it; 1 cites it directly.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names no predicate by number.

## Most influential descendants
- K212817: Merit Siege Vascular Plug (2021), 1 descendant of its own
- K240261: Siege Vascular Plug (SVP2.5-0.021); Siege Vascular Plug (SVP4-0.021); Siege Vascular Plug (SVP6-0.027) (2024), 0 descendants of its own

Source page: https://510kreport.com/device/K182944
Methodology: https://510kreport.com/methodology