# K904275: Morse Balloon Inflation Device

- Pathway: 510(k) (Traditional)
- Applicant: North American Instrument Corp.
- Decided: Jan 3, 1991 after 107 days
- Product code: MAV (Syringe, Balloon Inflation)
- 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.
11 later devices descend from it; 1 cites it directly.
0 of 12 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
- K953676: Breeze Digital Inflation Device (1996), 10 descendants of its own
- K022061: Cvsi Peripheral Balloon Catheter; Cvsi Inflater (2002), 9 descendants of its own
- K040155: Peripheral Cutting Balloon (2004), 6 descendants of its own
- K051254: Peripheral Cutting Balloon (2005), 5 descendants of its own
- K041993: 2 CM Peripheral Cutting Baloon (2004), 5 descendants of its own

Source page: https://510kreport.com/device/K904275
Methodology: https://510kreport.com/methodology