# K853095: Boehringer Laboratories Suction Intermittor

- Pathway: 510(k) (Traditional)
- Applicant: Boehringer Laboratories
- Decided: Aug 23, 1985 after 31 days
- Product code: GCX (Apparatus, Suction, Operating-Room, Wall Vacuum Powered)
- Device class: 2
- Regulation: 21 CFR 880.6740
- Recalls of this device: 3 (0 Class I)
- 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. FDA has not posted a summary or statement for it, so its predicates are not known.

## Recalls of this device
- Aug 1, 2005 · Not classified · Z-0156-06: Condition exists that prevents complete shutoff of the valve
- Aug 1, 2005 · Not classified · Z-0157-06: Condition exists that prevents complete shutoff of the valve
- Aug 1, 2005 · Not classified · Z-0155-06: Condition exists that prevents complete shutoff of the valve

Source page: https://510kreport.com/device/K853095
Methodology: https://510kreport.com/methodology