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FDA 510(k)

Kahook Dual Blade Glide (KDB Glide)

K-Number: K220891 · 2024-05-17

ApplicantNew World Medical, Inc.
Decision Date2024-05-17
Product CodeQUQ
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Kahook Dual Blade Glide (KDB Glide) is the device name listed in this FDA 510(k) record. The listed applicant is New World Medical, Inc.. It received FDA 510(k) clearance on 2024-05-17 under 510(k) number K220891. The device is classified under product code QUQ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Kahook Dual Blade Glide (KDB Glide)?

Kahook Dual Blade Glide (KDB Glide) is a medical device that received FDA 510(k) clearance on 2024-05-17. The listed applicant is New World Medical, Inc.. The 510(k) number is K220891.

When did Kahook Dual Blade Glide (KDB Glide) receive FDA 510(k) clearance?

Kahook Dual Blade Glide (KDB Glide) received FDA 510(k) clearance on 2024-05-17, under 510(k) number K220891.

Who is the listed applicant for Kahook Dual Blade Glide (KDB Glide)?

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

What is the FDA product code for Kahook Dual Blade Glide (KDB Glide)?

The FDA product code for Kahook Dual Blade Glide (KDB Glide) is QUQ.

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.

NCT07517302Kahook Dual Blade Goniotomy in Chronic Primary Angle-Closure GlaucomaRECRUITING

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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.

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