FDA 510(k) Applications Submitted by OHIO MEDICAL INSTRUMENT CO., INC.
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K021604 |
05/16/2002 |
MAYFIELD RADIOLUCENT SKULL PINS, MODEL 4-0-A-2020 |
OHIO MEDICAL INSTRUMENT CO., INC. |
K013428 |
10/16/2001 |
MAYFIELD/ACCISS OPERATING ARM SYSTEM AND MAYFIELD/OPTICAL ACCISS SYSTEM |
OHIO MEDICAL INSTRUMENT CO., INC. |
K960807 |
02/28/1996 |
TEW CRANIAL/SPINAL RETRACTOR MODEL A1090 |
OHIO MEDICAL INSTRUMENT CO., INC. |
K953124 |
07/05/1995 |
MAYFIELD RADIOLUCENT 2000 SKULL CLAMP |
OHIO MEDICAL INSTRUMENT CO., INC. |
K982244 |
06/25/1998 |
MAYFIELD ACCISS OPTICAL SYSTEM |
OHIO MEDICAL INSTRUMENT CO., INC. |
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. |
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