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FDA 510(k) Applications Submitted by KENNETH B 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.
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