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FDA 510(k)

Medline Cautery Electrode (PTFE)

K-Number: K173889 · 2018-04-09

ApplicantMedline Industries, Inc.
Decision Date2018-04-09
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Medline Cautery Electrode (PTFE) is a medical device manufactured by Medline Industries, Inc.. It received FDA 510(k) clearance on 2018-04-09 under approval number K173889. 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 Cautery Electrode (PTFE)?

Medline Cautery Electrode (PTFE) is a medical device that received FDA 510(k) clearance on 2018-04-09. It is manufactured by Medline Industries, Inc.. The 510(k) number is K173889.

When was Medline Cautery Electrode (PTFE) approved by the FDA?

Medline Cautery Electrode (PTFE) received FDA 510(k) clearance on 2018-04-09, under approval number K173889.

What company makes Medline Cautery Electrode (PTFE)?

Medline Cautery Electrode (PTFE) is manufactured by Medline Industries, Inc..

What is the FDA product code for Medline Cautery Electrode (PTFE)?

The FDA product code for Medline Cautery Electrode (PTFE) 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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