Phlebo Press DVT Model
K-Number: K172277 · 2017-11-03
ApplicantMego Afek AC , Ltd.
Decision Date2017-11-03
Product CodeJOW
Advisory CommitteeCV
DecisionSubstantially Equivalent
Device Summary
Phlebo Press DVT Model is a medical device manufactured by Mego Afek AC , Ltd.. It received FDA 510(k) clearance on 2017-11-03 under approval number K172277. 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 Phlebo Press DVT Model?
Phlebo Press DVT Model is a medical device that received FDA 510(k) clearance on 2017-11-03. It is manufactured by Mego Afek AC , Ltd.. The 510(k) number is K172277.
When was Phlebo Press DVT Model approved by the FDA?
Phlebo Press DVT Model received FDA 510(k) clearance on 2017-11-03, under approval number K172277.
What company makes Phlebo Press DVT Model?
Phlebo Press DVT Model is manufactured by Mego Afek AC , Ltd..
What is the FDA product code for Phlebo Press DVT Model?
The FDA product code for Phlebo Press DVT Model 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.