# K904667: NA Needles

- Pathway: 510(k) (Traditional)
- Applicant: Olympus Corp.
- Decided: Dec 12, 1990 after 58 days
- Product code: GDM (Needle, Aspiration And Injection, Reusable)
- 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.
67 later devices descend from it; 2 cite it directly.
1 of 68 devices in its family (counting itself) has 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
- K973128: Olympus NA-10J-1 Aspiration Needle (1997), 65 descendants of its own
- K023272: Disposable Aspiration Needle NA-200H (2002), 63 descendants of its own
- K050503: Single Use Aspiration Needle NA-201SX-4022 (2005), 28 descendants of its own
- K100712: Resound Endoscopic Ultrasound Aspiration Needle (2010), 27 descendants of its own
- K110030: Expect Endoscopic Aspiration Needle (2011), 26 descendants of its own

Source page: https://510kreport.com/device/K904667
Methodology: https://510kreport.com/methodology