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Avid N.I.T., Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
9
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K014246AVID-NIT NERVE STIMULATION NEEDLESJuly 16, 2002
K013231AVID-NIT PLASTIC HUB LUTZ EPIDURAL NEEDLE,MODEL RP2035L, AVID-NIT METAL HUB LUTZ EPIDURAL NEEDLE, MODecember 3, 2001
K983218N,I.T., INC. AUTOMATIC CUTTING BIOPSY NEEDLENovember 6, 1998
K972595ALDRETE EPIDURAL NEEDLE WITHOUT INTRODUCERMay 20, 1998
K972554REGANES RADIONUCLIDE SEED MAGAZINEFebruary 17, 1998
K973037N.I.T., INC. RADIONUCLIDE SEED APPLICATOR, MODEL SA-1000January 27, 1998
K973638N.I.T., INC. NEEDLE GUIDING TEMPLATEDecember 23, 1997
K971645REGANES SPINAL NEEDLE (VARIOUS)August 1, 1997
K945965ATRAUMATIC PENCIL POINT SPINAL NEEDLEAugust 2, 1995