PADLOCK CLIP EFTR Kit (00713229)
K-Number: K240274 · 2024-09-17
ApplicantSTERIS Corporation
Decision Date2024-09-17
Product CodePKL
Advisory CommitteeGU
DecisionSubstantially Equivalent
Device Summary
PADLOCK CLIP EFTR Kit (00713229) is a medical device manufactured by STERIS Corporation. It received FDA 510(k) clearance on 2024-09-17 under approval number K240274. The device is classified under product code PKL. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the PADLOCK CLIP EFTR Kit (00713229)?
PADLOCK CLIP EFTR Kit (00713229) is a medical device that received FDA 510(k) clearance on 2024-09-17. It is manufactured by STERIS Corporation. The 510(k) number is K240274.
When was PADLOCK CLIP EFTR Kit (00713229) approved by the FDA?
PADLOCK CLIP EFTR Kit (00713229) received FDA 510(k) clearance on 2024-09-17, under approval number K240274.
What company makes PADLOCK CLIP EFTR Kit (00713229)?
PADLOCK CLIP EFTR Kit (00713229) is manufactured by STERIS Corporation.
What is the FDA product code for PADLOCK CLIP EFTR Kit (00713229)?
The FDA product code for PADLOCK CLIP EFTR Kit (00713229) is PKL.
Other Devices by STERIS Corporation
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K182556SureClip Repositionable Hemostasis ClipMicro-Tech (Nanjing) Co., Ltd.
K180325Single Use MultiClip DeviceMicro-Tech (Nanjing) Co., Ltd.
K172727HemoclipHangzhou AGS MedTech Co., Ltd.
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.