510(k) K233917

Device
ICHOR 7F Embolectomy System (ICH-7F)
Applicant
Ichor
510(k) number
K233917
Product code
QEW
Decision
Substantially Equivalent (SESE)
Decision date
2024-07-18
Date received
2023-12-12
Regulation
870.5150
Classification name
Peripheral Mechanical Thrombectomy With Aspiration
Medical specialty
Cardiovascular
Review panel
Cardiovascular
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
N

Related Records

Applicant Contact

Contact
Timothy Blair
Address
1900 NW 25th St. Boca Raton FL US 33431 33431

FDA Registration Numbers

Source Documents

510(k) summary PDF

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