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)

BEST LOCALIZATION NEEDLE WITH I-125 SEED

K-Number: K122704 · 2013-01-09

ApplicantBest Medical Intl.
Decision Date2013-01-09
Product CodeKXK
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

BEST LOCALIZATION NEEDLE WITH I-125 SEED is the device name listed in this FDA 510(k) record. The listed applicant is Best Medical Intl.. It received FDA 510(k) clearance on 2013-01-09 under 510(k) number K122704. The device is classified under product code KXK. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BEST LOCALIZATION NEEDLE WITH I-125 SEED?

BEST LOCALIZATION NEEDLE WITH I-125 SEED is a medical device that received FDA 510(k) clearance on 2013-01-09. The listed applicant is Best Medical Intl.. The 510(k) number is K122704.

When did BEST LOCALIZATION NEEDLE WITH I-125 SEED receive FDA 510(k) clearance?

BEST LOCALIZATION NEEDLE WITH I-125 SEED received FDA 510(k) clearance on 2013-01-09, under 510(k) number K122704.

Who is the listed applicant for BEST LOCALIZATION NEEDLE WITH I-125 SEED?

The FDA 510(k) record lists Best Medical Intl. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BEST LOCALIZATION NEEDLE WITH I-125 SEED?

The FDA product code for BEST LOCALIZATION NEEDLE WITH I-125 SEED is KXK.

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

Related Devices (Code: KXK)

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.

K252296OncoPatchOncopatch, Inc.K242818IsoSphereIsoaid, LLCK223465RadianceTx Radionuclide Brachytherapy SourceRadiance Therapeutics, Inc.K221539GammaTileGt Medical TechnologiesK202267Sirius MRI Markers, Cs-131 Preloaded Strands with Sirius MRI Markers in 18 Gauge NeedlesIsoray Medical, Inc.K193602LV Liberty Vision Model 1 90Yttrium Brachytherapy SourceLv Liberty Vision Corporation

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.

↑