Home / 510(k) Clearances / K973037

510(k) K973037

N.I.T., INC. RADIONUCLIDE SEED APPLICATOR, MODEL SA-1000 by Avid N.I.T., Inc. — Product Code IWJ

K973037 is an FDA 510(k) premarket notification submitted by Avid N.I.T., Inc. for the device "N.I.T., INC. RADIONUCLIDE SEED APPLICATOR, MODEL SA-1000". The FDA issued a decision of Substantially Equivalent on January 27, 1998. The device falls under product code IWJ (System, Applicator, Radionuclide, Manual), a Class I device regulated under 21 CFR 892.5650. Avid N.I.T., Inc. has at least 8 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
January 27, 1998
Date Received
August 14, 1997
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
System, Applicator, Radionuclide, Manual
Device Class
Class I
Regulation Number
892.5650
Review Panel
RA
Submission Type

Other clearances by Avid N.I.T., Inc.

  • K014246 — AVID-NIT NERVE STIMULATION NEEDLES (July 16, 2002)
  • K013231 — AVID-NIT PLASTIC HUB LUTZ EPIDURAL NEEDLE,MODEL RP2035L, AVID-NIT METAL HUB LUTZ (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)
  • 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)

Other clearances for product code IWJ

  • K010166 — IMAGYN ISOSLEEVE / ISOSTAR NEEDLE SYSTEM (December 3, 2001)
  • K980997 — PGK DEVICE (MODIFIED) (September 28, 1998)
  • K972554 — REGANES RADIONUCLIDE SEED MAGAZINE (February 17, 1998)
  • K974118 — WORLDWIDE MEDICAL TECHNOLOGIES SEED IMPLANT NEEDLE SET (January 23, 1998)
  • K973786 — NORTHWEST RADIATION THERAPY PRODUCTS, PRECISION STEPPER AND GUIDE (January 2, 1998)
  • K973638 — N.I.T., INC. NEEDLE GUIDING TEMPLATE (December 23, 1997)
  • K973184 — PROSTATE SEEDING NEEDLE (November 21, 1997)
  • K963743 — MANAN PROSTATE UNI-LOCK (December 6, 1996)
  • K951052 — WEEKS APPLICATOR (August 22, 1996)
  • K961377 — MANAN PROSTATE LOCKING INTRODUCER SET (July 3, 1996)

FDA data resources