# K853312: Argon Cut Biopsy Needles, Various Sizes

- Pathway: 510(k) (Traditional)
- Applicant: Argon Medical Corp.
- Decided: Sep 12, 1985 after 36 days
- Product code: DWO (Needle, Biopsy, Cardiovascular)
- 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.
1 later device descends from it; 1 cites it directly.
0 of 2 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
- K214063: Model 121 Biopsy Needle, Model 111 Biopsy Needle, Model 112 Biopsy Needle, and Model 131 Disposable Coaxial Biopsy Needle (2022), 0 descendants of its own

Source page: https://510kreport.com/device/K853312
Methodology: https://510kreport.com/methodology