Lympha Press Optimal Plus
K-Number: K182003 · 2019-02-27
ApplicantMego Afek AC , Ltd.
Decision Date2019-02-27
Product CodeJOW
Advisory CommitteeCV
DecisionSubstantially Equivalent
Device Summary
Lympha Press Optimal Plus is a medical device manufactured by Mego Afek AC , Ltd.. It received FDA 510(k) clearance on 2019-02-27 under approval number K182003. The device is classified under product code JOW. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Lympha Press Optimal Plus?
Lympha Press Optimal Plus is a medical device that received FDA 510(k) clearance on 2019-02-27. It is manufactured by Mego Afek AC , Ltd.. The 510(k) number is K182003.
When was Lympha Press Optimal Plus approved by the FDA?
Lympha Press Optimal Plus received FDA 510(k) clearance on 2019-02-27, under approval number K182003.
What company makes Lympha Press Optimal Plus?
Lympha Press Optimal Plus is manufactured by Mego Afek AC , Ltd..
What is the FDA product code for Lympha Press Optimal Plus?
The FDA product code for Lympha Press Optimal Plus is JOW.
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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.