Utah Medical Products, Inc.

FDA 510(k) & PMA Approved Devices — 37 products

Total Devices37

Categories0

Latest FDA decision

Type	Number	Device Name	Code	Date	Actions
510(k)	K123310	FINESSE 3RD GENERATION (MODELS FINESSE+ AND FINESSEII+)	GEI	2013-01-23	View
510(k)	K101535	BT-CATH	OQY	2011-01-11	View
510(k)	K063611	SALINE/ CONTRAST MEDIA INFUSION CATHETER	LKF	2007-05-23	View
510(k)	K001874	PERIPHERALLY INSERTED CENTRAL CATHETER	LJS	2000-09-25	View
510(k)	K000974	FOWLER ENDOCURETTE, MODEL CUR-XXX	HHK	2000-05-23	View
510(k)	K965245	TBD	HGI	1997-07-03	View
510(k)	K970077	LIBERTY PLUS SYSTEM(PFS-300)/VAGINAL PROBE, LIBERTY PLUS(PFS-044)	KPI	1997-05-23	View
510(k)	K955663	ABC IN-LINE BLOOD SAMPLING KIT	CBT	1997-03-17	View
510(k)	K964526	LIBERTY RECTAL PELVIC FLOOR EXERCISER	KPI	1997-02-10	View
510(k)	K961424	INTRAN 500	HFN	1996-07-10	View
510(k)	K960496	LIBERTY LITE PFS SYSTEM	KPI	1996-06-27	View
510(k)	K955093	ASPIRATION/COAGULATION ELECTRODE ACE-311 & ACE-511	HGI	1996-04-29	View
510(k)	K960255	CERAMIC BLADE ELECTRODE	GEI	1996-03-27	View
510(k)	K955443	INTRAN PLUS	HFN	1996-02-20	View
510(k)	K954619	CORDGUARD II	KNA	1995-12-21	View
510(k)	K952981	FILTRESSE, SMOKE FILTRATION SYSTEM, 115 VAC & 230 VAC	FYD	1995-08-28	View
510(k)	K943448	LUMIN	LKF	1995-04-11	View
510(k)	K951032	FINESS I (DERMATOLOGIC APPLICATION)	GEI	1995-04-06	View
510(k)	K943250	LIBERTY	KPI	1995-02-09	View
510(k)	K941251	FINESSE IEC/601	HGI	1994-12-12	View