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 a medical device manufactured by New World Medical, Inc.. It received FDA 510(k) clearance on 2024-05-17 under approval 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. It is manufactured by New World Medical, Inc.. The 510(k) number is K220891.
When was Kahook Dual Blade Glide (KDB Glide) approved by the FDA?
Kahook Dual Blade Glide (KDB Glide) received FDA 510(k) clearance on 2024-05-17, under approval number K220891.
What company makes Kahook Dual Blade Glide (KDB Glide)?
Kahook Dual Blade Glide (KDB Glide) is manufactured by New World Medical, Inc..
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
Other Devices by New World Medical, Inc.
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.