ICHOR 7F Embolectomy System (ICH-7F)
K-Number: K233917 · 2024-07-18
Device Summary
Frequently Asked Questions
What is the ICHOR 7F Embolectomy System (ICH-7F)?
ICHOR 7F Embolectomy System (ICH-7F) is a medical device that received FDA 510(k) clearance on 2024-07-18. The listed applicant is Ichor. The 510(k) number is K233917.
When did ICHOR 7F Embolectomy System (ICH-7F) receive FDA 510(k) clearance?
ICHOR 7F Embolectomy System (ICH-7F) received FDA 510(k) clearance on 2024-07-18, under 510(k) number K233917.
Who is the listed applicant for ICHOR 7F Embolectomy System (ICH-7F)?
The FDA 510(k) record lists Ichor as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ICHOR 7F Embolectomy System (ICH-7F)?
The FDA product code for ICHOR 7F Embolectomy System (ICH-7F) is QEW.
Other records listing Ichor 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: QEW)
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.