# Alltek, Inc.

- Location (FDA's records): Nevada City, CA
- FDA decisions: 5 (1984–1985): 5 510(k) clearances
- Product codes: FPB (4), HQC (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K854172: I.V. Watch (Dec 5, 1985)
- K852030: Pediatric IV Watch (May 30, 1985)
- K852029: I.V. Watch (May 30, 1985)
- K840495: Manual Irrigating/Aspirating Unit (Jun 19, 1984)
- K834376: Filtrare TM Allvent TM (May 11, 1984)

Source page: https://510kreport.com/company/alltek