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FDA 510(k)

PHYSICIAN INDUSTRIES RADIOFREQUENCY ABLATION NEEDLE

K-Number: K040565 · 2004-07-22

ApplicantPhysician Industries, Inc.
Decision Date2004-07-22
Product CodeGXD
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

PHYSICIAN INDUSTRIES RADIOFREQUENCY ABLATION NEEDLE is the device name listed in this FDA 510(k) record. The listed applicant is Physician Industries, Inc.. It received FDA 510(k) clearance on 2004-07-22 under 510(k) number K040565. The device is classified under product code GXD. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PHYSICIAN INDUSTRIES RADIOFREQUENCY ABLATION NEEDLE?

PHYSICIAN INDUSTRIES RADIOFREQUENCY ABLATION NEEDLE is a medical device that received FDA 510(k) clearance on 2004-07-22. The listed applicant is Physician Industries, Inc.. The 510(k) number is K040565.

When did PHYSICIAN INDUSTRIES RADIOFREQUENCY ABLATION NEEDLE receive FDA 510(k) clearance?

PHYSICIAN INDUSTRIES RADIOFREQUENCY ABLATION NEEDLE received FDA 510(k) clearance on 2004-07-22, under 510(k) number K040565.

Who is the listed applicant for PHYSICIAN INDUSTRIES RADIOFREQUENCY ABLATION NEEDLE?

The FDA 510(k) record lists Physician Industries, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PHYSICIAN INDUSTRIES RADIOFREQUENCY ABLATION NEEDLE?

The FDA product code for PHYSICIAN INDUSTRIES RADIOFREQUENCY ABLATION NEEDLE is GXD.

Related Clinical Trials

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Other records listing Physician Industries, 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.

K033739PHYSICIAN INDUSTRIES' DURAMETER SYRINGEK960248GENERAL PROCEDURE KITK954068GENERAL HYGIENE KIT

Related Devices (Code: GXD)

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.

K251247GX1 Radiofrequency Generator Kit (RFG-X1-120V); GX1 Radiofrequency Generator Kit (RFG-X1-220V); GX1 Radiofrequency Generator Kit (RFG-X1-240V); GX1 System Release Rest of World (GX1-SYS-ROW); GX1 Radiofrequency Generator (51779845-01); GX1 Radiofrequency Generator (51779845-02); GX1 Radiofrequency Generator (51779845-03)Boston Scientific Neuromodulation CorporationK242057COOLIEF* Radiofrequency Generator (CRG-BASIC, CRG-BASIC-R, CRG-ADVANCED, CRG-ADVANCED-R)Avanos Medical, Inc.K232632Racz Neurostat RF GeneratorEpimed InternationalK231675OneRF Ablation SystemNeuroone Medical Technologies Corp.K220122APEX 6Rf Innovations, Inc.K203293Abbott Medical Grounding Pad, model RF-DGP-ISABBOTT MEDICAL

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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