# K875117: Ciba Corning Balanced Heparin for CA++

- Pathway: 510(k) (Traditional)
- Applicant: Ciba Corning Diagnostics Corp.
- Decided: Feb 29, 1988 after 76 days
- Product code: CBT (Arterial Blood Sampling Kit)
- Device class: 1
- Regulation: 21 CFR 868.1100
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
4 later devices descend from it; 1 cites it directly.
0 of 5 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
- K982922: Vacutainer Brand Blood Collection Syringe (1998), 3 descendants of its own
- K022426: BD Preset Blood Collection Syringe, BD a-Line Blood Collection Syringe, Models 365313, 365323,365316,365356,365373,36538 (2002), 2 descendants of its own
- K260128: BD Preset™ and BD A-Line™ Arterial Blood Collection Syringes (2026), 0 descendants of its own
- K202446: BD Preset Syringe & BD A-Line Syringe (2020), 0 descendants of its own

Source page: https://510kreport.com/device/K875117
Methodology: https://510kreport.com/methodology