Phlebo Press DVT Model
K-Number: K172277 · 2017-11-03
Device Summary
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. The listed applicant is Mego Afek AC , Ltd.. The 510(k) number is K172277.
When did Phlebo Press DVT Model receive FDA 510(k) clearance?
Phlebo Press DVT Model received FDA 510(k) clearance on 2017-11-03, under 510(k) number K172277.
Who is the listed applicant for Phlebo Press DVT Model?
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 Phlebo Press DVT Model?
The FDA product code for Phlebo Press DVT Model 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.