# K050656: Amsino Suture Removal Kit

- Pathway: 510(k) (Traditional)
- Applicant: Amsino International, Inc.
- Decided: May 2, 2005 after 49 days
- Product code: MCZ (Suture Removal Kit)
- Device class: 1
- Regulation: 21 CFR 878.4800
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device 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.

## Indications for use
The AMSINO® Suture Removal Kit is intended for use in suture removal procedures.

Source page: https://510kreport.com/device/K050656
Methodology: https://510kreport.com/methodology