FDA 510(k) Applications Submitted by Jean Asquith

FDA 510(k) Number Submission Date Device Name Applicant
K100385 02/16/2010 NUBY NATURAL TOUCH RHYTHM DUAL ACTION ELECTRIC BREAST PUMP LUV N' CARE, LTD.
K090646 03/11/2009 CARDIOTECH SPIROMETRY SYSTEM, MODEL GT-105 CHEST M.I., INC.
K090821 03/26/2009 CHEX SINGLE USE CURVED INTRALUMINAL CIRCULAR STAPLER, MODEL CS 21, CS 25, CS 28, CS 32, CS 21L, CS 25L, CS 28L, CS 32L FRANKENMAN INTERNATIONAL LIMITED
K101378 05/17/2010 FRANKENMAN SURGICAL STAPLERS SUZHOU FRANKENMAN MEDICAL EQUIPMENT CO., LTD.
K081965 07/10/2008 MPOWRX SNORING SOLUTION MPOWRX HEALTH AND WELLNESS PRODUCTS INC.
K202006 07/21/2020 ENT Plasma Wands, Turbinator Wand, Werewolf Irrigation Tube Set, Werewolf ENT Adapter, Werewolf Coblation System ArthroCare Corporation
K092240 07/23/2009 ACUPUNCTURE NEEDLES HAENGLIM SEOWON MEDICAL CO.
K092731 09/04/2009 VIBRO-TRAC PNEUMEX, INC.
K093100 10/01/2009 REVLON RVSP3501 SPA MOISTURESTAY PARAFFIN BATH (TYPE SPB3752EA) SHENZHEN COMFORT TECHNOLOGY CO., LTD.
K033664 11/21/2003 MODIFICATION TO ALLOCLASSIC ZWEYMULLER SL OFFSET FEMORAL STEM CENTERPULSE ORTHOPEDICS, INC.
K083560 12/02/2008 EXPANDED SPECTRUM PHOTO THERAPY DEVICE, MODEL ESPT-3X LIGHTHOUSE TECHNICAL INNOVATIONS, INC.


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