# K882383: Maggi Series Ultra. Needle, Biopsy/Catheter Guides

- Pathway: 510(k) (Traditional)
- Applicant: CIVCO Medical Instruments Co., Inc.
- Decided: Nov 28, 1988 after 172 days
- Product code: DWZ (Device, Biopsy, Endomyocardial)
- Device class: 2
- Regulation: 21 CFR 870.4075
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
368 later devices descend from it; 4 cite it directly.
2 of 369 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
- K974432: Ultraguide 1000 (1998), 358 descendants of its own
- K023227: USG 2000SA (2002), 280 descendants of its own
- K053610: Abaris (2006), 278 descendants of its own
- K121498: Percunav (2012), 222 descendants of its own
- K132304: Epiq Diagnostic Ultrasound System (2013), 211 descendants of its own

Source page: https://510kreport.com/device/K882383
Methodology: https://510kreport.com/methodology