# K112828: Revive Intermediate Catheter (Revive IC)

- Pathway: 510(k) (Special)
- Applicant: Codman & Shurtleff, Inc.
- Decided: Oct 25, 2011 after 27 days
- Product code: DQY (Catheter, Percutaneous)
- 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: 3 generations back to K960806 (1996). 4 ancestors in all.
No later device cites it as a predicate yet.
0 of 5 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K982770: 6F Envoy Guiding Catheter, Cordis Corp. (1998) Summary page 1.
- K060116: Micrus Courier Microcatheters, Micrus Endovascular Corporation (2006) Summary page 1.

## Indications for use
The REVIVE M Intermediate Catheter is intended for use in the peripheral, coronary, and neurovasculature for the intravascular introduction of interventional/diagnostic devices.

Source page: https://510kreport.com/device/K112828
Methodology: https://510kreport.com/methodology