# Midwest City Hearing Aid Center

- Location (FDA's records): Midwest City, OK
- FDA decisions: 12 (1995–1997): 12 510(k) clearances
- Product codes: ESD (12)
- 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
- K970430: Adaptive Compression - Class D/ Class D Agci (Mar 11, 1997)
- K963604: Dynamic EQ II - 2 Channel Wide Dynamic Range Compression (Sep 27, 1996)
- K963607: Horizon 1 and 2 Programable Full Shell and in the Canal (Sep 20, 1996)
- K953729: K Amp Full Shell and in the Ear (Sep 12, 1995)
- K953728: RX12 Linear Full Shell and in the Canal (Sep 12, 1995)
- K953631: Snip Input Compression Class a (Aug 28, 1995)
- K952986: Spi-Secret Personal Instrument Cic (Aug 7, 1995)
- K953036: DB Push-Pull Hearing Aid (Jul 21, 1995)

Source page: https://510kreport.com/company/midwest-city-hearing-aid-center