# K953522: Usci Ideal Ptca Kit

- Pathway: 510(k) (Traditional)
- Applicant: Ryder Intl. Corp.
- Decided: Apr 17, 1996 after 265 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.
13 later devices descend from it; 2 cite it directly.
0 of 14 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) Merit Medical Systems Monarch™ Balloon Catheter inflation Syringe: named in the summary without a submission number

## Most influential descendants
- K962611: Bard Eagle Inflation Device (1996), 12 descendants of its own
- K972964: Atrion Medical Balloon Catheter Inflation Device (1997), 11 descendants of its own
- K032840: Atrion Medical QL Inflation Device (2004), 6 descendants of its own
- K020333: Atrion Medical QL Fluid Dispensing Syringe (2002), 2 descendants of its own
- K103231: Kyphon Inflation Syringe (2011), 1 descendant of its own

## Indications for use
The Ryder device is intended for single use inflating of a balloon catheter, monitoring the pressure within the catheter and deflating the balloon catheter during angioplasty procedures.

Source page: https://510kreport.com/device/K953522
Methodology: https://510kreport.com/methodology