FDA 510(k) Applications Submitted by KIM E AVES

FDA 510(k) Number Submission Date Device Name Applicant
K970376 02/03/1997 PTCA GUIDEWIRE LAKE REGION MFG., INC.
K970994 03/19/1997 CORE AND COIL ASSEMBLY GUIDEWIRE LAKE REGION MFG., INC.
K971322 04/10/1997 CORE AND COIL ASSEMBLY GUIDEWIRE LAKE REGION MFG., INC.
K031891 06/13/2003 VIRTUOSAPH TERUMO CARDIOVASCULAR SYSTEMS CORP.
K960718 02/21/1996 LRM LAKE REGION MFG., INC.
K960866 03/04/1996 LRM PRODUCES GUIDEWIRES ON AN OEM BASIS FOR MANUFACTURERS,KIT ASSEMBLERS, AND DISTRIBUTORS. LAKE REGION MFG., INC.
K981326 04/13/1998 LAKE REGION MANUFACTURING GUIDEWIRES LAKE REGION MFG., INC.
K981667 05/11/1998 HYDROPHILIC COATED GUIDEWIRE LAKE REGION MFG., INC.
K041324 05/18/2004 CALMATRIX CALCIUM SULFATE BONE GRAFT BINDER LIFECORE BIOMEDICAL, INC.
K192900 10/15/2019 H500 Multi-Sensing Oximetry System Nonin Medical, Inc.
K160231 02/01/2016 Model X-100C CO-MetÖ Oximetry System NONIN MEDICAL, INC.
K172625 09/01/2017 Reusable, Finger Clip Nonin Medical CO-Met Oximetry Sensor Nonin Medical Inc.


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