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Company · US

Armour Pharmaceutical Co.

FDA 510(k) clearances and medical device recalls filed under this name, 1984 to 1984. Name variants (Inc, Corp, punctuation) are merged.

7510(k) clearances (0 in 12 months)

0recalls (0 in 12 months)

0recalls that name a 510(k)

Product codes

Code	Device	Records
CCQ	Nebulizer, Medicinal, Non-Ventilatory (Atomizer)	5
BZE	Heater, Breathing System W/Wo Controller (Not Humidifier Or Nebulizer	1
LDR	Controller, Infusion, Intravascular, Electronic	1

Latest 510(k) clearances

Decided	510(k)	Device and applicant	Code
Dec 4, 1984	K842209	ARM-A-FLOW INTRAVENOUS FLOW REGULATOR Armour Pharmaceutical Co.	LDR
Nov 8, 1984	K844005	ARM-A-VIAL LV HEATER-BREATHING SYS Armour Pharmaceutical Co.	BZE
Jul 27, 1984	K841991	ARM-A-CARE HUMIDIFIER-RESPIRATORY GAS Armour Pharmaceutical Co.	CCQ
Jul 27, 1984	K841990	ARM-A-CARE NEBULIZER-NEBULIZER Armour Pharmaceutical Co.	CCQ
Jul 27, 1984	K841989	ARM-A-VIAL LV SODIUM CHLORIDE INHALAT Armour Pharmaceutical Co.	CCQ
Jul 27, 1984	K841988	ARM-A-VIAL LV SODIUM, CHLORIDE INHALAT Armour Pharmaceutical Co.	CCQ
Jul 27, 1984	K841987	ARM-A-VIAL LV STERIAL WATER FOR INHALA Armour Pharmaceutical Co.	CCQ

Latest recalls

Date	Firm and product	Code	Linked 510(k)
No recalls in this window.

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