FDA 510(k) Applications Submitted by KENNETH G MILLER

FDA 510(k) Number	Submission Date	Device Name	Applicant
K982244	06/25/1998	MAYFIELD ACCISS OPTICAL SYSTEM	OHIO MEDICAL INSTRUMENT CO., INC.
K122857	09/18/2012	HOPE CONTINUOUS NEBULIZER MODEL HOPE-11310, HEART NEBULIZER MODEL HEART-100609, THERAMIST NEBULIZER MODEL THERAMIST-3100	PEGASUS RESEARCH CORP.
K991267	04/13/1999	SPINE APPLICATIONS FOR THE MAYFIELD/ACCISS OPERATING ARM AND OPTICAL ACCISS SYSTEMS MODULE, MAYFIELD/ACCISS SPINE RING A	OHIO MEDICAL INSTRUMENT CO., INC.
K992843	08/24/1999	THE MAYFIELD / ACCISS SYSTEM WITH WINDOWS NT FOR CRANIAL SURGERY, THE MAYFIELD / OPTICAL ACCISS SYSTEM WITH WINDOWS NT F	OHIO MEDICAL INSTRUMENT CO., INC.
K983282	09/18/1998	OMI OCCIPITAL CERVICAL LOOP, MODEL A1089	OHIO MEDICAL INSTRUMENT CO., INC.
K020700	03/04/2002	PMH 5000 HEATED HUMIDIFIER FOR RESPIRATORY THERAPY	PEGASUS RESEARCH CORP.
K013856	11/06/2001	PMH 1000 HEATED HUMIDIFIER	PEGASUS RESEARCH CORP.