Avid N.I.T., Inc. is one of 15071 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Avid N.I.T., Inc. - FDA 510(k) Cleared Devices
Recent clearances: N,I.T., INC. AUTOMATIC CUTTING BIOPSY NEEDLE, ALDRETE EPIDURAL NEEDLE WITHOUT INTRODUCER, REGANES RADIONUCLIDE SEED MAGAZINE
9
Total
9
Cleared
0
Denied
Avid N.I.T., Inc. has 9 FDA 510(k) cleared medical devices. Based in Tarpon Springs, US.
Historical record: 9 cleared submissions from 1995 to 2002. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Avid N.I.T., Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Spectra Medical Devices, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Avid N.I.T., Inc.
9 devices
Cleared
Jul 16, 2002
AVID-NIT NERVE STIMULATION NEEDLES
Anesthesiology
202d
Cleared
Dec 03, 2001
AVID-NIT PLASTIC HUB LUTZ EPIDURAL NEEDLE,MODEL RP2035L, AVID-NIT METAL HUB...
Anesthesiology
67d
Cleared
Nov 06, 1998
N,I.T., INC. AUTOMATIC CUTTING BIOPSY NEEDLE
Gastroenterology & Urology
53d
Cleared
May 20, 1998
ALDRETE EPIDURAL NEEDLE WITHOUT INTRODUCER
Anesthesiology
313d
Cleared
Feb 17, 1998
REGANES RADIONUCLIDE SEED MAGAZINE
Radiology
224d
Cleared
Jan 27, 1998
N.I.T., INC. RADIONUCLIDE SEED APPLICATOR, MODEL SA-1000
Radiology
166d
Cleared
Dec 23, 1997
N.I.T., INC. NEEDLE GUIDING TEMPLATE
Radiology
90d
Cleared
Aug 01, 1997
REGANES SPINAL NEEDLE (VARIOUS)
Anesthesiology
88d
Cleared
Aug 02, 1995
ATRAUMATIC PENCIL POINT SPINAL NEEDLE
Anesthesiology
238d