# K982839: Cadd-Legacy Pca Ambulatory Infusion System, Model 6300

- Pathway: 510(k) (Traditional)
- Applicant: Sims Deltec, Inc.
- Decided: Nov 2, 1998 after 82 days
- Product code: MEA (Pump, Infusion, Pca)
- Device class: 2
- Regulation: 21 CFR 880.5725
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
3 later devices descend from it; 2 cite it directly.
2 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) CADD-PCA® Ambulatory Infusion Pump: named in the summary without a submission number
- (no number) CADD-Prizm® VIP Model 6100 Ambulatory Infusion System: named in the summary without a submission number

## Most influential descendants
- K140783: Halo Ambulatory Infusion System (2014), 1 descendant of its own
- K153193: Halo II Ambulatory Infusion System (also with trade names Nimbus II Ambulatory Infusion System, EVAA Ambulatory Infusion System) (2016), 0 descendants of its own
- K013822: Microjet Crono Pca (2002), 0 descendants of its own

## Indications for use
The CADD-Legacy™ pump is suitable for intravenous, intra-arterial, subcutaneous, intraperitoneal, epidural space, or subarachnoid space infusion.

Source page: https://510kreport.com/device/K982839
Methodology: https://510kreport.com/methodology