Maxq-Al , Ltd. is one of 267 FDA 510(k) medical device manufacturers from Israel in the dataset, ranked by real submission volume.
Maxq-Al , Ltd. has 2 FDA 510(k) cleared medical devices. Based in Tel Aviv, IL.
Historical record: 2 cleared submissions from 2018 to 2020. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Maxq-Al , Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Maxq AL , Ltd. as regulatory consultant.
FDA 510(k) Regulatory Record - Maxq-Al , Ltd.
2 devices