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FDA 510(k)

LCCS INSULATED SPINAL NEEDLE (RF CANNULA)

K-Number: K112231 · 2011-08-19

ApplicantLccs Products Limited
Decision Date2011-08-19
Product CodeGXI
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

LCCS INSULATED SPINAL NEEDLE (RF CANNULA) is the device name listed in this FDA 510(k) record. The listed applicant is Lccs Products Limited. It received FDA 510(k) clearance on 2011-08-19 under 510(k) number K112231. The device is classified under product code GXI. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LCCS INSULATED SPINAL NEEDLE (RF CANNULA)?

LCCS INSULATED SPINAL NEEDLE (RF CANNULA) is a medical device that received FDA 510(k) clearance on 2011-08-19. The listed applicant is Lccs Products Limited. The 510(k) number is K112231.

When did LCCS INSULATED SPINAL NEEDLE (RF CANNULA) receive FDA 510(k) clearance?

LCCS INSULATED SPINAL NEEDLE (RF CANNULA) received FDA 510(k) clearance on 2011-08-19, under 510(k) number K112231.

Who is the listed applicant for LCCS INSULATED SPINAL NEEDLE (RF CANNULA)?

The FDA 510(k) record lists Lccs Products Limited as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LCCS INSULATED SPINAL NEEDLE (RF CANNULA)?

The FDA product code for LCCS INSULATED SPINAL NEEDLE (RF CANNULA) is GXI.

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 Lccs Products Limited 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.

K191293LCCS VC-S RF CannulaK152642LCCS Disposable RF Electrode, LCCS Reusable RF ElectrodeK131006ANESTHESIA CONDUCTION NEEDLESK132136SINGLE USE GROUNDING PAD

Related Devices (Code: GXI)

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.

K253907Disposable Radiofrequency CannulaABBOTT MEDICALK251802STAR RF Ablation SystemMerit Medical Systems, Inc.K251243OneRF Trigeminal Nerve Radiofrequency ProbesNeuroone Medical Technologies Corp.K242841Disposable RF Electrode (RFDE-5/RFDE-10/RFDE-15/RFDE-20)ABBOTT MEDICALK250213OptaBlate BVN Intraosseous Nerve Ablation System (10mm Probe Single Kit); OptaBlate BVN Intraosseous Nerve Ablation System (10mm Probe Dual Kit)Stryker InstrumentsK241367RF CannulaShanghai Samedical & Plastic Instruments Co., Ltd.

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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