FDA 510(k) Applications Submitted by AVID N.I.T., INC.
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. |
K013231 |
09/27/2001 |
AVID-NIT PLASTIC HUB LUTZ EPIDURAL NEEDLE,MODEL RP2035L, AVID-NIT METAL HUB LUTZ EPIDURAL NEEDLE, MODEL RM2035L |
AVID N.I.T., INC. |
K014246 |
12/26/2001 |
AVID-NIT NERVE STIMULATION NEEDLES |
AVID N.I.T., INC. |
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