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FDA 510(k)

Abbott Medical Grounding Pad, model RF-DGP-IS

K-Number: K203293 · 2022-01-21

ApplicantABBOTT MEDICAL
Decision Date2022-01-21
Product CodeGXD
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

Abbott Medical Grounding Pad, model RF-DGP-IS is the device name listed in this FDA 510(k) record. The listed applicant is ABBOTT MEDICAL. It received FDA 510(k) clearance on 2022-01-21 under 510(k) number K203293. 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 Abbott Medical Grounding Pad, model RF-DGP-IS?

Abbott Medical Grounding Pad, model RF-DGP-IS is a medical device that received FDA 510(k) clearance on 2022-01-21. The listed applicant is ABBOTT MEDICAL. The 510(k) number is K203293.

When did Abbott Medical Grounding Pad, model RF-DGP-IS receive FDA 510(k) clearance?

Abbott Medical Grounding Pad, model RF-DGP-IS received FDA 510(k) clearance on 2022-01-21, under 510(k) number K203293.

Who is the listed applicant for Abbott Medical Grounding Pad, model RF-DGP-IS?

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

What is the FDA product code for Abbott Medical Grounding Pad, model RF-DGP-IS?

The FDA product code for Abbott Medical Grounding Pad, model RF-DGP-IS is GXD.

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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.K201610IonicRF GeneratorABBOTT 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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