# K982077: Selector Diagnostic Catheter

- Pathway: 510(k) (Traditional)
- Applicant: Boston Scientific Scimed, Inc.
- Decided: Aug 11, 1998 after 60 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: 2 generations back to K922552 (1993). 5 ancestors in all.
No later device cites it as a predicate yet.
0 of 6 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K960801: Selector Angiographic Catheter (Various Models), North American Instrument Corp. (1996) Summary page 1.
- K960975: 1-4F Infiniti Angiographic Catheter, Cordis Corp. (1996) Summary page 1.

## Cited in the summary but kept off the family tree
- K925522: Centrysystem 3 with Charts/BP Option, C.G.H. Medical, Inc. (1994). Our OCR of the scanned summary read K925522, FDA’s number for Centrysystem 3 with Charts/BP Option (C.G.H. Medical, Inc.). Its FDA name has none of the distinctive words the summary uses for the device it names, “5 French and 6 French SELECTOR™ diagnostic catheters”. Kept off the family tree. Summary page 1.

## Indications for use
The 4 French SELECTOR™ diagnostic catheter is designed to deliver contrast medium during angiography as well as to provide a conduit for various diagnostic and therapeutic procedures.

Source page: https://510kreport.com/device/K982077
Methodology: https://510kreport.com/methodology