Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Applications Submitted by Neuravi Ltd.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K173452
11/06/2017
EmboTrap ll Revascularization Device
Neuravi Ltd.
K211338
05/03/2021
EMBOTRAP III Revascularization Device
Neuravi Ltd.
K212908
09/13/2021
EmboTrap II Revascularization Device, EMBOTRAP III Revascularization Device
Neuravi Ltd.
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact