# K932249: Durasafe B-D Combined Spinal Epidural Anesthesia

- Pathway: 510(k) (Traditional)
- Applicant: Bd Becton Dickinson Vacutainer Systems Preanalytic
- Decided: Aug 27, 1993 after 109 days
- Product code: CAZ (Anesthesia Conduction Kit)
- Device class: 2
- Regulation: 21 CFR 868.5140
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
42 later devices descend from it; 3 cite it directly.
0 of 43 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
- K954953: B-D Durasafe Combined Spinal Epidural (Cse) Tray (1996), 39 descendants of its own
- K040965: Pajunk Tuohy Needles, Quincke Needles, Chiba Needles & Crawford Needles (2004), 36 descendants of its own
- K113207: Sono Tap, Tuohy Sono (2012), 11 descendants of its own
- K070354: Imd's Anesthesia Needles (Tuohy, Quincke and Pencil Point) (2007), 7 descendants of its own
- K131006: Anesthesia Conduction Needles (2013), 5 descendants of its own

Source page: https://510kreport.com/device/K932249
Methodology: https://510kreport.com/methodology