# K882796: Slip-Coat (TM) Catheters

- Pathway: 510(k) (Traditional)
- Applicant: Cook, Inc.
- Decided: Jul 28, 1988 after 22 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
No predicates in its family tree.
15 later devices descend from it; 3 cite it directly.
4 of 16 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K122937: Slip-Cath Beacon Tip Catheter Model SCBR (Product Prefix), Shuttle Select Slip-Cath Catheter Model SCBR (Product Prefix) (2012), 9 descendants of its own
- K071468: Clarivein Catheter (2008), 4 descendants of its own
- K153502: ClariVein IC (2016), 3 descendants of its own
- K201907: ClariVein IC (2020), 2 descendants of its own
- K162448: White Sizing Catheter, Aurous Centimeter Sizing Catheter, Cava Vessel Sizing Catheter (2017), 1 descendant of its own

Source page: https://510kreport.com/device/K882796
Methodology: https://510kreport.com/methodology