# Aerscher Diagnostics

- Location (FDA's records): Chestertown, MD
- FDA decisions: 3 (1997–2003): 3 510(k) clearances
- Product codes: KHE (3)
- 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
- K031356: Hemaprompt Gastric (Sep 24, 2003)
- K981661: Hemaprompt (Sep 15, 1998)
- K972763: Hemaprompt (Oct 20, 1997)

Source page: https://510kreport.com/company/aerscher-diagnostics