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Company · US

Omnicon Medical Corp.

FDA 510(k) clearances and medical device recalls filed under this name, 1976 to 1983. Name variants (Inc, Corp, punctuation) are merged.

10510(k) clearances (0 in 12 months)

0recalls (0 in 12 months)

0recalls that name a 510(k)

Product codes

Code	Device	Records
CAH	Filter, Bacterial, Breathing-Circuit	5
CAI	Circuit, Breathing (W Connector, Adaptor, Y Piece)	2
CAE	Airway, Oropharyngeal, Anesthesiology	1
EWC	Chamber, Acoustic (For Audiometric Testing)	1
FMP	Protector, Skin Pressure	1

Latest 510(k) clearances

Decided	510(k)	Device and applicant	Code
Jan 21, 1983	K823872	EMERGENCY TRACHEOSTOMY KIT Omnicon Medical Corp.	EWC
Mar 18, 1982	K820577	ANESTHESIA BACTERIA FILTER Omnicon Medical Corp.	CAH
Mar 18, 1982	K820576	MAINFLOW BACTERIA FILTER Omnicon Medical Corp.	CAH
Aug 13, 1980	K801804	ANESTHESIA BACTERIA FILTER Omnicon Medical Corp.	CAH
Aug 13, 1980	K801803	MAINFLOW BACTERIA FILTER Omnicon Medical Corp.	CAH
Dec 20, 1977	K772060	PROTECT IV GARD Omnicon Medical Corp.	FMP
Feb 14, 1977	K770136	DISPOSABLE BACTERIA FILTER Omnicon Medical Corp.	CAH
Jan 12, 1977	K770001	AIRWAY, BERMAN 40, 60, 80, 90, L00MM'S Omnicon Medical Corp.	CAE
Oct 27, 1976	K760819	CONDUCTIVE ANESTHESIA BREATHING CIRCUIT Omnicon Medical Corp.	CAI
Jul 19, 1976	K760149	CONDUCTIVE ANESTHSIA BREATH. CIRCUIT Omnicon Medical Corp.	CAI

Latest recalls

Date	Firm and product	Code	Linked 510(k)
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