Lympha Press Optimal Plus
K-Number: K170658 · 2017-05-31
Device Summary
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 2017-05-31. The listed applicant is Mego Afek AC , Ltd.. The 510(k) number is K170658.
When did Lympha Press Optimal Plus receive FDA 510(k) clearance?
Lympha Press Optimal Plus received FDA 510(k) clearance on 2017-05-31, under 510(k) number K170658.
Who is the listed applicant for Lympha Press Optimal Plus?
The FDA 510(k) record lists Mego Afek AC , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Lympha Press Optimal Plus?
The FDA product code for Lympha Press Optimal Plus is JOW.
Other records listing Mego Afek AC , Ltd. as applicant
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.
Related Devices (Code: JOW)
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.
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.