# K090167: Philips Avent Classic Stage 2 and 3 Teether, Model SCF882/01, SCF884/01, Philips Avent Animal Stage 2 and 3 Teether,

- Pathway: 510(k) (Traditional)
- Applicant: Philips Electronics UK Limited
- Decided: Jun 18, 2009 after 147 days
- Product code: KKO (Ring, Teething, Fluid-Filled)
- Device class: 2
- Regulation: 21 CFR 872.5550
- 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. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

Source page: https://510kreport.com/device/K090167
Methodology: https://510kreport.com/methodology