FDA 510(k)

Abbott Medical Grounding Pad, model RF-DGP-IS

K-Number: K203293 · 2022-01-21

Decision Date2022-01-21

Product CodeGXD

Advisory CommitteeNE

DecisionSubstantially Equivalent

Device Summary

Abbott Medical Grounding Pad, model RF-DGP-IS is a medical device manufactured by ABBOTT MEDICAL. It received FDA 510(k) clearance on 2022-01-21 under approval 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. It is manufactured by ABBOTT MEDICAL. The 510(k) number is K203293.

When was Abbott Medical Grounding Pad, model RF-DGP-IS approved by the FDA?

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

What company makes Abbott Medical Grounding Pad, model RF-DGP-IS?

Abbott Medical Grounding Pad, model RF-DGP-IS is manufactured by ABBOTT MEDICAL.

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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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.