# K960801: Selector Angiographic Catheter (Various Models)

- Pathway: 510(k) (Traditional)
- Applicant: North American Instrument Corp.
- Decided: Mar 29, 1996 after 31 days
- Product code: DQO (Catheter, Intravascular, Diagnostic)
- Device class: 2
- Regulation: 21 CFR 870.1200
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K922552 (1993). 1 ancestor in all.
1 later device descends from it; 1 cites it directly.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K922552: Morse (R) Angiographic Catheters, North American Instrument Corp. (1993) Summary page 1.

## Most influential descendants
- K982077: Selector Diagnostic Catheter (1998), 0 descendants of its own

## Indications for use
The Selector Angiographic Catheter is intended to deliver contrast medium during angiography as well as to provide a conduit for various diagnostic and therapeutic procedures. Selector Angiographic Catheters are intended for single-patient use only.

Source page: https://510kreport.com/device/K960801
Methodology: https://510kreport.com/methodology