FDA 510(k) Applications Submitted by JOSEPH E HARMS
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K971645 |
05/05/1997 |
REGANES SPINAL NEEDLE (VARIOUS) |
AVID N.I.T., INC. |
K972554 |
07/08/1997 |
REGANES RADIONUCLIDE SEED MAGAZINE |
AVID N.I.T., INC. |
K972595 |
07/11/1997 |
ALDRETE EPIDURAL NEEDLE WITHOUT INTRODUCER |
AVID N.I.T., INC. |
K973037 |
08/14/1997 |
N.I.T., INC. RADIONUCLIDE SEED APPLICATOR, MODEL SA-1000 |
AVID N.I.T., INC. |
K983218 |
09/14/1998 |
N,I.T., INC. AUTOMATIC CUTTING BIOPSY NEEDLE |
AVID N.I.T., INC. |
K973638 |
09/24/1997 |
N.I.T., INC. NEEDLE GUIDING TEMPLATE |
AVID N.I.T., INC. |
|
|