# Alerchek, Inc.

- Location (FDA's records): Portland, ME
- FDA decisions: 3 (1986–1989): 3 510(k) clearances
- Product codes: DHB (2), DGC (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
- K885307: Flipscreen (TM) Total E Immunoassay (Mar 8, 1989)
- K874802: Flipscreen Qat (Feb 17, 1988)
- K860027: Flipscreen Specific E (PE, SE, NE, SW, NW) Assay (Apr 22, 1986)

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