Padlock Clip defect closure system, Padlock Pro-Select defect closure device
K-Number: K192722 · 2019-10-24
ApplicantSTERIS Corporation
Decision Date2019-10-24
Product CodePKL
Advisory CommitteeGU
DecisionSubstantially Equivalent
Device Summary
Padlock Clip defect closure system, Padlock Pro-Select defect closure device is a medical device manufactured by STERIS Corporation. It received FDA 510(k) clearance on 2019-10-24 under approval number K192722. 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 defect closure system, Padlock Pro-Select defect closure device?
Padlock Clip defect closure system, Padlock Pro-Select defect closure device is a medical device that received FDA 510(k) clearance on 2019-10-24. It is manufactured by STERIS Corporation. The 510(k) number is K192722.
When was Padlock Clip defect closure system, Padlock Pro-Select defect closure device approved by the FDA?
Padlock Clip defect closure system, Padlock Pro-Select defect closure device received FDA 510(k) clearance on 2019-10-24, under approval number K192722.
What company makes Padlock Clip defect closure system, Padlock Pro-Select defect closure device?
Padlock Clip defect closure system, Padlock Pro-Select defect closure device is manufactured by STERIS Corporation.
What is the FDA product code for Padlock Clip defect closure system, Padlock Pro-Select defect closure device?
The FDA product code for Padlock Clip defect closure system, Padlock Pro-Select defect closure device is PKL.
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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.