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FDA 510(k)

I-PLANT MODEL 3500 (125IODINE BRACHYTHERAPY SEEDS)-STERILE

K-Number: K023242 · 2002-12-04

ApplicantImplant Sciences Corp.
Decision Date2002-12-04
Product CodeKXK
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

I-PLANT MODEL 3500 (125IODINE BRACHYTHERAPY SEEDS)-STERILE is the device name listed in this FDA 510(k) record. The listed applicant is Implant Sciences Corp.. It received FDA 510(k) clearance on 2002-12-04 under 510(k) number K023242. 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 I-PLANT MODEL 3500 (125IODINE BRACHYTHERAPY SEEDS)-STERILE?

I-PLANT MODEL 3500 (125IODINE BRACHYTHERAPY SEEDS)-STERILE is a medical device that received FDA 510(k) clearance on 2002-12-04. The listed applicant is Implant Sciences Corp.. The 510(k) number is K023242.

When did I-PLANT MODEL 3500 (125IODINE BRACHYTHERAPY SEEDS)-STERILE receive FDA 510(k) clearance?

I-PLANT MODEL 3500 (125IODINE BRACHYTHERAPY SEEDS)-STERILE received FDA 510(k) clearance on 2002-12-04, under 510(k) number K023242.

Who is the listed applicant for I-PLANT MODEL 3500 (125IODINE BRACHYTHERAPY SEEDS)-STERILE?

The FDA 510(k) record lists Implant Sciences Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for I-PLANT MODEL 3500 (125IODINE BRACHYTHERAPY SEEDS)-STERILE?

The FDA product code for I-PLANT MODEL 3500 (125IODINE BRACHYTHERAPY SEEDS)-STERILE 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

Other records listing Implant Sciences Corp. 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.

K070468IMPLANT SCIENCES CORP. MODEL HDR 4454K042864IMPLANT SCIENCES CORP, MODEL HDR-4140K023073SEED LINKK994317I-PLANT, MODEL 3500K990193IODINE BRACHYTHERAPY SEEDS, MODEL 3000

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

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

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