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FDA 510(k)

Medline Universal Grounding Pad

K-Number: K212093 · 2022-01-14

ApplicantMedline Industries, Inc.
Decision Date2022-01-14
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Medline Universal Grounding Pad is a medical device manufactured by Medline Industries, Inc.. It received FDA 510(k) clearance on 2022-01-14 under approval number K212093. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Medline Universal Grounding Pad?

Medline Universal Grounding Pad is a medical device that received FDA 510(k) clearance on 2022-01-14. It is manufactured by Medline Industries, Inc.. The 510(k) number is K212093.

When was Medline Universal Grounding Pad approved by the FDA?

Medline Universal Grounding Pad received FDA 510(k) clearance on 2022-01-14, under approval number K212093.

What company makes Medline Universal Grounding Pad?

Medline Universal Grounding Pad is manufactured by Medline Industries, Inc..

What is the FDA product code for Medline Universal Grounding Pad?

The FDA product code for Medline Universal Grounding Pad is GEI.

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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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