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FDA 510(k)

Medline Cautery Tip Cleaner

K-Number: K210526 · 2021-03-12

Decision Date2021-03-12
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Medline Cautery Tip Cleaner is the device name listed in this FDA 510(k) record. The listed applicant is Medline Industries, Inc.. It received FDA 510(k) clearance on 2021-03-12 under 510(k) number K210526. 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 Tip Cleaner?

Medline Cautery Tip Cleaner is a medical device that received FDA 510(k) clearance on 2021-03-12. The listed applicant is Medline Industries, Inc.. The 510(k) number is K210526.

When did Medline Cautery Tip Cleaner receive FDA 510(k) clearance?

Medline Cautery Tip Cleaner received FDA 510(k) clearance on 2021-03-12, under 510(k) number K210526.

Who is the listed applicant for Medline Cautery Tip Cleaner?

The FDA 510(k) record lists Medline Industries, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Medline Cautery Tip Cleaner?

The FDA product code for Medline Cautery Tip Cleaner is GEI.

Related Clinical Trials

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.

Other records listing Medline Industries, Inc. 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.

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Related Devices (Code: GEI)

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.

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.