FDA 510(k) Applications Submitted by Kristy Mo

FDA 510(k) Number Submission Date Device Name Applicant
K222548 08/23/2022 Endo Motor Shenzhen Perfect Medical Instruments Co., Ltd.
K991991 06/14/1999 DUPEL IONTOPHORESIS SYSTEM EMPI
K013517 10/22/2001 10600 DEFLECTABLE CATHETER SYSTEM, MODEL 10600 MEDTRONIC VASCULAR
K033989 12/23/2003 MEDTRONIC SELECTSITE DEFLECTABLE CATHETER SYSTEM, MODELS C304-S59 AND C304-L69 MEDTRONIC INC. CARDIAC RHYTHM MANAGEMENT


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