# K120738: Flash Pta Balloon Dilatation Catheter-4.0X14MMX135CM

- Pathway: 510(k) (Special)
- Applicant: Ostial Corporation
- Decided: Mar 29, 2012 after 17 days
- Product code: LIT (Catheter, Angioplasty, Peripheral, Transluminal)
- Device class: 2
- Regulation: 21 CFR 870.1250
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 5 generations back to K001134 (2000). 5 ancestors in all.
4 later devices descend from it; 3 cite it directly.
0 of 10 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K102482: Flash Pta Balloon Dilatation Catheter 5MM X 19MM X 135CM; Flash Pta Balloon Dilatation Catheter 6MM X 19MM X 135CM, Ostial Corporation (2011)

## Most influential descendants
- K121175: Flash Pta Ballon Dilatation Catheter-5MM X 19MM X 135CM (2012), 3 descendants of its own
- K122379: Flash Pta Balloon Dilatation Catheter - 4MM X 14MM X 135CM, Flash Pta Balloon Dilatation Catheter - 4MM X 19MM X 135CM (2012), 2 descendants of its own
- K133861: Flash Ostial System Otw-7.0MMX17MMX135CM, Flash Ostial System Otw-7.0MMX17MMX80CM (2014), 1 descendant of its own
- K150946: FLASH Ostial System OTW-6.0mm x 12mm x 80cm, FLASH Ostial System OTW-6.0mm x 12mm x 135cm, FLASH Ostial System OTW-7.0mm x 12mm x 80cm, FLASH Ostial System OTW-7.0mm x 12mm x 135cm (2015), 0 descendants of its own

## Indications for use
The Flash PTA Balloon Dilatation Catheter is indicated for use in Percutaneous Transluminal Angioplasty in the peripheral vasculature at aorto-ostial locations, including iliac, renal and carotid arteries. This catheter is not intended for use in coronary arteries.

Source page: https://510kreport.com/device/K120738
Methodology: https://510kreport.com/methodology