# K870523: Hawkins Breast Localization Needle

- Pathway: 510(k) (Traditional)
- Applicant: N-S Medical Products
- Decided: Mar 9, 1987 after 31 days
- Product code: GDM (Needle, Aspiration And Injection, Reusable)
- Device class: 1
- Regulation: 21 CFR 878.4800
- Recalls of this device: 1 (0 Class I)
- 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. FDA has not posted a summary or statement for it, so its predicates are not known.

## Recalls of this device
- Sep 1, 2009 · Not classified · Z-2015-2010: Medical Device Technologies doing business as Angiotech has conducted a recall on Angiotech Breast Localization Needles, Soft Tissue Biopsy Needles, Vascular Access Needles, Bone Biopsy Needles, Acces

Source page: https://510kreport.com/device/K870523
Methodology: https://510kreport.com/methodology