Armour Pharmaceutical Co. - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Armour Pharmaceutical Co. has 7 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 7 cleared submissions from 1984 to 1984. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Armour Pharmaceutical Co. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Armour Pharmaceutical Co.
7 devices
Cleared
Dec 04, 1984
ARM-A-FLOW INTRAVENOUS FLOW REGULATOR
General Hospital
183d
Cleared
Nov 08, 1984
ARM-A-VIAL LV HEATER-BREATHING SYS
Anesthesiology
27d
Cleared
Jul 27, 1984
ARM-A-VIAL LV STERIAL WATER FOR INHALA
Anesthesiology
86d
Cleared
Jul 27, 1984
ARM-A-VIAL LV SODIUM, CHLORIDE INHALAT
Anesthesiology
79d
Cleared
Jul 27, 1984
ARM-A-VIAL LV SODIUM CHLORIDE INHALAT
Anesthesiology
79d
Cleared
Jul 27, 1984
ARM-A-CARE NEBULIZER-NEBULIZER
Anesthesiology
79d
Cleared
Jul 27, 1984
ARM-A-CARE HUMIDIFIER-RESPIRATORY GAS
Anesthesiology
79d