# K102648: Ant Inflation Device/Ant Inflation Device Compact Pack

- Pathway: 510(k) (Traditional)
- Applicant: Shenzhen Ant Hi-Tech Industrial Co., Ltd.
- Decided: Jul 1, 2011 after 290 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
Longest line of descent: 3 generations back to K872981 (1987). 4 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 6 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K962495: Indeflator Plus 30/Plus 30 Priority PACK9WITH the.096 or.115 Rotating Hemostatic Valve), Advanced Cardiovascular Systems, Inc. (1996) Summary page 1.

## Most influential descendants
- K133795: Summed Inflation Device Kit (2014), 0 descendants of its own

## Indications for use
The ANT Inflation Device is intended for use during vascular procedures in conjunction with interventional device such as balloon catheters to create and monitor pressure in the balloon catheter. The ANT Inflation Device Compact Pack: -ANT Inflation Device: See description above. -ANT Inflation Device Accessory Kit: The Accessory Kit is recommended for use during vascular procedures in conjunction and/or diagnostic device (e.g., balloon dilatation catheters, adtherectomy devices, sent delivery systems, intravascular urtrasound devices.)

Source page: https://510kreport.com/device/K102648
Methodology: https://510kreport.com/methodology