Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

Owen Mumford USA, Inc.

FDA 510(k) & PMA Approved Devices — 10 products

Total Devices10

Categories0

Latest FDA decision

Type	Number	Device Name	Code	Date	Actions
510(k)	K013362	AUTOJECT 2	KZH	2001-11-13	View
510(k)	K993385	AUTOJET 2 (NON-FIXED NEEDLE TYPE)	KZH	1999-11-10	View
510(k)	K983994	UNIFINE	FMF	1999-01-08	View
510(k)	K983974	OWEN MUMFORD 3ML AUTOPEN	FMF	1998-12-21	View
510(k)	K982275	RAPPORT V.T.D.	LKY	1998-12-04	View
510(k)	K983045	AMIELLE	KXP	1998-11-25	View
510(k)	K973899	UNIFINE PENTIPS	FMI	1997-12-04	View
510(k)	K971443	RAPPORT V.T.D.	LKY	1997-09-26	View
510(k)	K953735	AUTOJECT MINI	KZH	1995-11-08	View
510(k)	K945660	AUTOJECT 2	KZH	1995-08-11	View

↑