# K922033: Saline Solution- Sterile

- Pathway: 510(k) (Traditional)
- Applicant: Trinity Laboratories, Inc.
- Decided: Jul 21, 1992 after 81 days
- Product code: CCQ (Nebulizer, Medicinal, Non-Ventilatory (Atomizer))
- Device class: 1
- Regulation: 21 CFR 868.5640
- 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. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K981905: Sterile Saline Solution 0.9%- Catalog NO, 10290, Sterile Water- Catalog NO. 10291 (1998), 0 descendants of its own

Source page: https://510kreport.com/device/K922033
Methodology: https://510kreport.com/methodology