Argosy Intl. (Usa), Inc.
Argosy Intl. (Usa), Inc. holds FDA 510(k) medical device clearances, first cleared 1978, most recent 1982.
Top product codes for Argosy Intl. (Usa), Inc.
Recent clearances by Argosy Intl. (Usa), Inc.
- K823075 — REXTON
- K791548 — REXTON HS(HEARING SYSTEM)
- K781094 — HEARING AID, EYEGLASS
- K781095 — HEARING AID, BEHIND THE EAR
- K781096 — HEARING AID, EYEGLASS, B-12
- K780914 — PM 25 PP (BODY AID)
- K780915 — 780 SE (BEHIND THE EAR)
- K780916 — 780 UE (BEHIND THE EAR)
- K780917 — PRIMO CE (BEHIND THE EAR)
- K780918 — PRIMO CEDM (BEHIND THE EAR)
- K780919 — M25 PP (BEHIND THE EAR)
- K780920 — MM-CE 11 (BEHIND THE EAR)
- K780921 — MM-CE DM (BEHIND THE EAR)
- K780922 — UM VII (BEHIND THE EAR)
Data sourced from openFDA. This site is unofficial and independent of the FDA.