# K963839: Cordis Suction Reservoir - Model Number: 910-500

- Pathway: 510(k) (Traditional)
- Applicant: Cordis Corp.
- Decided: Dec 12, 1996 after 79 days
- Product code: GCY (Apparatus, Suction, Single Patient Use, Portable, Nonpowered)
- Device class: 1
- Regulation: 21 CFR 878.4680
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) Sil-Med Suction Reservoir: named in the summary without a submission number
- (no number) Cordis Integral Drainage/Ventricular/Lumbar Drainage Sets: named in the summary without a submission number

## Indications for use
The Cordis Suction Reservoir Kit is intended to be used with the Cordis Subdural Drainage Catheter for drainage of extraventricular fluid collections.

Source page: https://510kreport.com/device/K963839
Methodology: https://510kreport.com/methodology