Gn Danavox, Inc.
Gn Danavox, Inc. holds FDA 510(k) medical device clearances, first cleared 1986, most recent 1997.
Top product codes for Gn Danavox, Inc.
Recent clearances by Gn Danavox, Inc.
- K971031 — AUDALLION III HEARING SYSTEM
- K971032 — DANAVOX MODELS 163/162 BTE
- K942331 — DANAVOX MODEL CIC
- K924185 — DFS GENIUS BTE
- K905679 — 133 SERIES BTE
- K905692 — 143 SERIES BTE
- K896996 — CAS (COMPUTERIZED ANALYZER SYSTEM)
- K896995 — DISCRETION, IN THE CANAL HEARING INSTRUMENT
- K891594 — CERUMEN FILTER
- K863975 — CUSTOM IN-THE-EAR
Data sourced from openFDA. This site is unofficial and independent of the FDA.