# K963648: Stryker Suction Regulator

- Pathway: 510(k) (Traditional)
- Applicant: Stryker Endoscopy
- Decided: Nov 26, 1996 after 75 days
- Product code: GCX (Apparatus, Suction, Operating-Room, Wall Vacuum Powered)
- Device class: 2
- Regulation: 21 CFR 880.6740
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
1 later device descends from it; 1 cites it directly.
0 of 2 devices 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) Arthrex Suction Regulator: named in the summary without a submission number

## Most influential descendants
- K030307: Davol Arthrovent Outflow Tubing (2003), 0 descendants of its own

## Indications for use
It is intended for uses in any procedure in which the control of suction force is desired.

Source page: https://510kreport.com/device/K963648
Methodology: https://510kreport.com/methodology