Ashai Co. , Ltd. - FDA 510(k) Cleared Devices
12
Total
12
Cleared
0
Denied
Ashai Co. , Ltd. has 12 FDA 510(k) cleared anesthesiology devices. Based in Australia, AU.
Historical record: 12 cleared submissions from 1985 to 1987.
Browse the complete list of FDA 510(k) cleared anesthesiology devices from this manufacturer. Filter by specialty or product code using the sidebar.
12 devices
Cleared
May 15, 1987
AEROSOL ONE, NEBULIZER PUMP
Anesthesiology
101d
Cleared
Apr 24, 1986
AEROSOL ONE
Anesthesiology
308d
Cleared
Oct 31, 1985
SAFE.N.SURE
Obstetrics & Gynecology
133d
Cleared
Sep 26, 1985
MAXI-NEB
Anesthesiology
98d
Cleared
Sep 18, 1985
OXY-DIAL
Anesthesiology
90d
Cleared
Sep 18, 1985
OXY-ONE
Anesthesiology
90d
Cleared
Sep 18, 1985
OXY-TWO
Anesthesiology
90d
Cleared
Sep 18, 1985
OXY-TUBE
Anesthesiology
90d
Cleared
Sep 18, 1985
AERO-MASK ONE
Anesthesiology
90d
Cleared
Sep 18, 1985
NASAL ONE
Anesthesiology
90d
Cleared
Sep 18, 1985
AERO-MASK TWO
Anesthesiology
90d
Cleared
Aug 27, 1985
URI-SURE
Gastroenterology & Urology
68d