# K872981: Acs Indeflator Plus (Modification #2)

- Pathway: 510(k) (Traditional)
- Applicant: Advanced Cardiovascular Systems, Inc.
- Decided: Oct 20, 1987 after 81 days
- Product code: DXT (Injector And Syringe, Angiographic)
- Device class: 2
- Regulation: 21 CFR 870.1650
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
10 later devices descend from it; 2 cite it directly.
0 of 11 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
- K961471: Indeflator 20/30 Inflation Device and 20/30 Priority Pack (with the .096 or .115 Rotating Hemostatic Valve) (1996), 9 descendants of its own
- K042449: Dolphin Inflation Device (2005), 5 descendants of its own
- K082755: Sedat Flamingo (2008), 3 descendants of its own
- K962495: Indeflator Plus 30/Plus 30 Priority PACK9WITH the.096 or.115 Rotating Hemostatic Valve) (1996), 3 descendants of its own
- K152387: Fluent Inflation Device (2015), 1 descendant of its own

Source page: https://510kreport.com/device/K872981
Methodology: https://510kreport.com/methodology