# Dahlberg Electronics, Inc.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 31 (1979–1990): 31 510(k) clearances
- Product codes: ESD (31)
- 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
- K896159: Dahlberg Model LP Behind-the-Ear Hearing Aid (Jan 22, 1990)
- K896157: Dahlberg Model LH Behind-the-Ear Hearing Aid (Jan 22, 1990)
- K896158: Dahlberg Model LA Behind-the-Ear Hearing Aid (Jan 22, 1990)
- K881417: Dahlberg Model GP Body Aid (Jun 7, 1988)
- K881612: Dahlberg Model XJ 8080 Body-Worn Hearing Aid (Jun 1, 1988)
- K874831: Audiotone Model A2000 Behind-the-Ear Hearing Aid (Feb 22, 1988)
- K874830: Miracle Ear Model BP Behind-the-Ear Hearing Aid (Feb 17, 1988)
- K873169: Dahlberg Model GH Body Aid (Sep 16, 1987)

Source page: https://510kreport.com/company/dahlberg-electronics