Avid N.I.T., Inc.
Avid N.I.T., Inc. appears in FDA public data with 0 recalls, 9 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on July 16, 2002.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 9
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K014246 | AVID-NIT NERVE STIMULATION NEEDLES | July 16, 2002 |
| K013231 | AVID-NIT PLASTIC HUB LUTZ EPIDURAL NEEDLE,MODEL RP2035L, AVID-NIT METAL HUB LUTZ EPIDURAL NEEDLE, MO | December 3, 2001 |
| K983218 | N,I.T., INC. AUTOMATIC CUTTING BIOPSY NEEDLE | November 6, 1998 |
| K972595 | ALDRETE EPIDURAL NEEDLE WITHOUT INTRODUCER | May 20, 1998 |
| K972554 | REGANES RADIONUCLIDE SEED MAGAZINE | February 17, 1998 |
| K973037 | N.I.T., INC. RADIONUCLIDE SEED APPLICATOR, MODEL SA-1000 | January 27, 1998 |
| K973638 | N.I.T., INC. NEEDLE GUIDING TEMPLATE | December 23, 1997 |
| K971645 | REGANES SPINAL NEEDLE (VARIOUS) | August 1, 1997 |
| K945965 | ATRAUMATIC PENCIL POINT SPINAL NEEDLE | August 2, 1995 |