Argosy Intl. (Usa), Inc. - FDA 510(k) Cleared Devices
14
Total
14
Cleared
0
Denied
Argosy Intl. (Usa), Inc. has 14 FDA 510(k) cleared ear, nose, throat devices. Based in Mchenry, US.
Historical record: 14 cleared submissions from 1978 to 1982.
Browse the complete list of FDA 510(k) cleared ear, nose, throat devices from this manufacturer. Filter by specialty or product code using the sidebar.
14 devices
Cleared
Nov 08, 1982
REXTON
Gastroenterology & Urology
20d
Cleared
Sep 28, 1979
REXTON HS(HEARING SYSTEM)
Orthopedic
46d
Cleared
Jul 17, 1978
HEARING AID, EYEGLASS
Ear, Nose, Throat
17d
Cleared
Jul 17, 1978
HEARING AID, BEHIND THE EAR
Ear, Nose, Throat
17d
Cleared
Jul 17, 1978
HEARING AID, EYEGLASS, B-12
Ear, Nose, Throat
17d
Cleared
Jun 14, 1978
PM 25 PP (BODY AID)
Ear, Nose, Throat
9d
Cleared
Jun 14, 1978
780 SE (BEHIND THE EAR)
Ear, Nose, Throat
9d
Cleared
Jun 14, 1978
780 UE (BEHIND THE EAR)
Ear, Nose, Throat
9d
Cleared
Jun 14, 1978
PRIMO CE (BEHIND THE EAR)
Ear, Nose, Throat
9d
Cleared
Jun 14, 1978
PRIMO CEDM (BEHIND THE EAR)
Ear, Nose, Throat
9d
Cleared
Jun 14, 1978
M25 PP (BEHIND THE EAR)
Ear, Nose, Throat
9d
Cleared
Jun 14, 1978
MM-CE 11 (BEHIND THE EAR)
Ear, Nose, Throat
9d