Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

REGANES RADIONUCLIDE SEED MAGAZINE

K-Number: K972554 · 1998-02-17

ApplicantAvid N.I.T., Inc.
Decision Date1998-02-17
Product CodeIWJ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

REGANES RADIONUCLIDE SEED MAGAZINE 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 1998-02-17 under 510(k) number K972554. 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 REGANES RADIONUCLIDE SEED MAGAZINE?

REGANES RADIONUCLIDE SEED MAGAZINE is a medical device that received FDA 510(k) clearance on 1998-02-17. The listed applicant is Avid N.I.T., Inc.. The 510(k) number is K972554.

When did REGANES RADIONUCLIDE SEED MAGAZINE receive FDA 510(k) clearance?

REGANES RADIONUCLIDE SEED MAGAZINE received FDA 510(k) clearance on 1998-02-17, under 510(k) number K972554.

Who is the listed applicant for REGANES RADIONUCLIDE SEED MAGAZINE?

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 REGANES RADIONUCLIDE SEED MAGAZINE?

The FDA product code for REGANES RADIONUCLIDE SEED MAGAZINE 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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

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 INTRODUCERK973037N.I.T., INC. RADIONUCLIDE SEED APPLICATOR, MODEL SA-1000K973638N.I.T., INC. NEEDLE GUIDING TEMPLATE

View all 9 devices →

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.K973037N.I.T., INC. RADIONUCLIDE SEED APPLICATOR, MODEL SA-1000Avid 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.

↑