510(k) K212988

Device
ONO Retrieval Device
Applicant
Onocor Vascular, LLC
510(k) number
K212988
Product code
MMX
Decision
Substantially Equivalent (SESE)
Decision date
2022-05-23
Date received
2021-09-20
Regulation
870.5150
Classification name
Device, Percutaneous Retrieval
Medical specialty
Cardiovascular
Review panel
Cardiovascular
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
No

Applicant Contact#

Contact
Tiffini Wittwer
Address
808 General Sterling Dr. West Chester PA US 19382 19382

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

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