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FDA 510(k)

STRYKER INTERVENTIONAL PAIN RF GENERATOR

K-Number: K032601 · 2004-04-01

ApplicantValley Forge Scientific Corp.
Decision Date2004-04-01
Product CodeGXD
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

STRYKER INTERVENTIONAL PAIN RF GENERATOR is the device name listed in this FDA 510(k) record. The listed applicant is Valley Forge Scientific Corp.. It received FDA 510(k) clearance on 2004-04-01 under 510(k) number K032601. 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 STRYKER INTERVENTIONAL PAIN RF GENERATOR?

STRYKER INTERVENTIONAL PAIN RF GENERATOR is a medical device that received FDA 510(k) clearance on 2004-04-01. The listed applicant is Valley Forge Scientific Corp.. The 510(k) number is K032601.

When did STRYKER INTERVENTIONAL PAIN RF GENERATOR receive FDA 510(k) clearance?

STRYKER INTERVENTIONAL PAIN RF GENERATOR received FDA 510(k) clearance on 2004-04-01, under 510(k) number K032601.

Who is the listed applicant for STRYKER INTERVENTIONAL PAIN RF GENERATOR?

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

What is the FDA product code for STRYKER INTERVENTIONAL PAIN RF GENERATOR?

The FDA product code for STRYKER INTERVENTIONAL PAIN RF GENERATOR is GXD.

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Other records listing Valley Forge Scientific 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.

K050364MALIS 2000 BIPOLAR ELECTROSURGICAL SYSTEMK042604VALLY FORGE SCIENTIFIC MALIS BIPOLAR DISPOSABLE FINGER OPERATED ELECTROSURGICAL INSTRUMENTSK033499MALIS IRRIGATION MODULE 1000K982229BI-DENTK973554VALLEY FORGE BIPOLAR BALL TIP ELECTRODEK971986VALLEY FORGE BIPOLAR LOOP

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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

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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