# K230281: Picoclamp

- Pathway: 510(k) (Traditional)
- Applicant: Kono Seisakusho Co., Ltd.
- Decided: Oct 23, 2023 after 264 days
- Product code: DXC (Clamp, Vascular)
- Device class: 2
- Regulation: 21 CFR 870.4450
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 2 generations back to K961100 (1996). 2 ancestors in all.
No later device cites it as a predicate yet.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K161315: Vein Clamps, Artery Clamps, Aros Surgical Instruments Corporation (2016) Summary page 5.

## Indications for use
A surgical instrument used to occlude a blood vessel temporarily.

Source page: https://510kreport.com/device/K230281
Methodology: https://510kreport.com/methodology