FDA 510(k) Applications Submitted by UTAH MEDICAL PRODUCTS, INC.

FDA 510(k) Number Submission Date Device Name Applicant
K123310 10/25/2012 FINESSE 3RD GENERATION (MODELS FINESSE+ AND FINESSEII+) UTAH MEDICAL PRODUCTS, INC.
K143424 12/01/2014 UTAH CVX-RIPE UTAH MEDICAL PRODUCTS, INC.
K960255 01/17/1996 CERAMIC BLADE ELECTRODE UTAH MEDICAL PRODUCTS, INC.
K960496 02/01/1996 LIBERTY LITE PFS SYSTEM UTAH MEDICAL PRODUCTS, INC.
K964526 11/12/1996 LIBERTY RECTAL PELVIC FLOOR EXERCISER UTAH MEDICAL PRODUCTS, INC.
K955663 12/13/1995 ABC IN-LINE BLOOD SAMPLING KIT UTAH MEDICAL PRODUCTS, INC.
K965245 12/31/1996 TBD UTAH MEDICAL PRODUCTS, INC.
K955093 11/07/1995 ASPIRATION/COAGULATION ELECTRODE ACE-311 & ACE-511 UTAH MEDICAL PRODUCTS, INC.
K101535 06/03/2010 BT-CATH UTAH MEDICAL PRODUCTS, INC.
K000974 03/27/2000 FOWLER ENDOCURETTE, MODEL CUR-XXX UTAH MEDICAL PRODUCTS, INC.
K961424 04/12/1996 INTRAN 500 UTAH MEDICAL PRODUCTS, INC.
K001874 06/20/2000 PERIPHERALLY INSERTED CENTRAL CATHETER UTAH MEDICAL PRODUCTS, INC.
K955443 11/28/1995 INTRAN PLUS UTAH MEDICAL PRODUCTS, INC.
K063611 12/03/2006 SALINE/ CONTRAST MEDIA INFUSION CATHETER UTAH MEDICAL PRODUCTS, INC.
K970077 01/09/1997 LIBERTY PLUS SYSTEM(PFS-300)/VAGINAL PROBE, LIBERTY PLUS(PFS-044) UTAH MEDICAL PRODUCTS, INC.


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