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FDA 510(k)

N.I.T., INC. RADIONUCLIDE SEED APPLICATOR, MODEL SA-1000

K-Number: K973037 · 1998-01-27

ApplicantAvid N.I.T., Inc.
Decision Date1998-01-27
Product CodeIWJ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

N.I.T., INC. RADIONUCLIDE SEED APPLICATOR, MODEL SA-1000 is the device name listed in this FDA 510(k) record. The listed applicant is Avid N.I.T., Inc.. It received FDA 510(k) clearance on 1998-01-27 under 510(k) number K973037. The device is classified under product code IWJ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the N.I.T., INC. RADIONUCLIDE SEED APPLICATOR, MODEL SA-1000?

N.I.T., INC. RADIONUCLIDE SEED APPLICATOR, MODEL SA-1000 is a medical device that received FDA 510(k) clearance on 1998-01-27. The listed applicant is Avid N.I.T., Inc.. The 510(k) number is K973037.

When did N.I.T., INC. RADIONUCLIDE SEED APPLICATOR, MODEL SA-1000 receive FDA 510(k) clearance?

N.I.T., INC. RADIONUCLIDE SEED APPLICATOR, MODEL SA-1000 received FDA 510(k) clearance on 1998-01-27, under 510(k) number K973037.

Who is the listed applicant for N.I.T., INC. RADIONUCLIDE SEED APPLICATOR, MODEL SA-1000?

The FDA 510(k) record lists Avid N.I.T., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for N.I.T., INC. RADIONUCLIDE SEED APPLICATOR, MODEL SA-1000?

The FDA product code for N.I.T., INC. RADIONUCLIDE SEED APPLICATOR, MODEL SA-1000 is IWJ.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Other records listing Avid N.I.T., Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K014246AVID-NIT NERVE STIMULATION NEEDLESK013231AVID-NIT PLASTIC HUB LUTZ EPIDURAL NEEDLE,MODEL RP2035L, AVID-NIT METAL HUB LUTZ EPIDURAL NEEDLE, MODEL RM2035LK983218N,I.T., INC. AUTOMATIC CUTTING BIOPSY NEEDLEK972595ALDRETE EPIDURAL NEEDLE WITHOUT INTRODUCERK972554REGANES RADIONUCLIDE SEED MAGAZINEK973638N.I.T., INC. NEEDLE GUIDING TEMPLATE

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Related Devices (Code: IWJ)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K010166IMAGYN ISOSLEEVE / ISOSTAR NEEDLE SYSTEMImagyn Medical Technologies, Inc.K980997PGK DEVICE (MODIFIED)Pgk, Inc.K972554REGANES RADIONUCLIDE SEED MAGAZINEAvid N.I.T., Inc.K974118WORLDWIDE MEDICAL TECHNOLOGIES SEED IMPLANT NEEDLE SETWorldwide Medical Technologies, LLCK973786NORTHWEST RADIATION THERAPY PRODUCTS, PRECISION STEPPER AND GUIDENw Radiation Therapy ProductsK973638N.I.T., INC. NEEDLE GUIDING TEMPLATEAvid N.I.T., Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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