# K851026: Moi-Stir Oral Swabstick (S)

- Pathway: 510(k) (Traditional)
- Applicant: Kingswood Laboratories, Inc.
- Decided: May 21, 1985 after 70 days
- Product code: LFD (Saliva, Artificial)
- Device class: U
- Recalls of this device: 1 (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
- Apr 22, 2005 · Not classified · Z-0820-05: Contaminated with Aspergillus and Penicillum molds.

Source page: https://510kreport.com/device/K851026
Methodology: https://510kreport.com/methodology