# K790472: Burron Vented Needle

- Pathway: 510(k) (Traditional)
- Applicant: National Patent Development Corp.
- Decided: Mar 26, 1979 after 21 days
- Product code: GAA (Needle, Aspiration And Injection, Disposable)
- 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.
13 later devices descend from it; 1 cites it directly.
2 of 14 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
- K013087: Single Dose Dispensing Pin, Model 2201 (2001), 12 descendants of its own
- K040634: Robertsite Vial Adapter, Model 245700021 (2004), 5 descendants of its own
- K071307: Invirolink  and Inviro Tip Blunt Cannulas, Model 130001, 130501, 140001, 140002, 140003 (2008), 2 descendants of its own
- K072759: VIAL2BAG (2007), 2 descendants of its own
- K140730: VIAL2BAG Direct Connect (2014), 1 descendant of its own

Source page: https://510kreport.com/device/K790472
Methodology: https://510kreport.com/methodology