# K954925: Bactec Lytic/10 Anaerobic/F Culture Vials

- Pathway: 510(k) (Traditional)
- Applicant: Becton Dickinson Diagnostic Instrument Systems
- Decided: Feb 16, 1996 after 113 days
- Product code: MDB (System, Blood Culturing)
- Device class: 1
- Regulation: 21 CFR 866.2560
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
2 later devices descend from it; 2 cite it directly.
0 of 3 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
- K141810: BD Bactec Plus Anaerobic/F (Plastic) (2014), 0 descendants of its own
- K123903: BACTEC Lytic/10 Anaerobic/F Culture Vials (plastic) (2013), 0 descendants of its own

Source page: https://510kreport.com/device/K954925
Methodology: https://510kreport.com/methodology