FDA 510(k) Applications Submitted by CHARLES E DINKLER II
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K001342 |
04/27/2000 |
P.O.P. PAIN KIT |
POST OPERATIVE PAIN MANAGEMENT |
K071480 |
05/29/2007 |
LIAISON 25 OH VITAMIN D TOTAL; ASSAY, CONTROL SET AND SPECIMEN DILUENT SET, MODELS 310600, 310601 AND 310602 |
DIASORIN, INC. |
K050319 |
02/09/2005 |
MAYFIELD MR/CT SKULL CLAMP, MODEL 4-0-A-1104 |
INTEGRA LIFESCIENCES CORP. |
K021604 |
05/16/2002 |
MAYFIELD RADIOLUCENT SKULL PINS, MODEL 4-0-A-2020 |
OHIO MEDICAL INSTRUMENT CO., INC. |
K073163 |
11/09/2007 |
LIMITED ARTIFACT SKULL PIN, MODEL 0107 |
DINKLER SURGICAL DEVICES, INC. |
K090695 |
03/16/2009 |
DINKLER SURGICAL SKULL CLAMP, MODEL 0308 |
DINKLER SURGICAL DEVICES, INC. |
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