Pristine Access Technologies , Ltd. is one of 267 FDA 510(k) medical device manufacturers from Israel in the dataset, ranked by real submission volume.
Pristine Access Technologies , Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Pristine Hemodialysis Catheter
1
Total
1
Cleared
0
Denied
Pristine Access Technologies , Ltd. has 1 FDA 510(k) cleared medical devices. Based in Tel-Aviv, IL.
Historical record: 1 cleared submissions from 2019 to 2019. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Pristine Access Technologies , Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Orly Maor as regulatory consultant.
FDA 510(k) Regulatory Record - Pristine Access Technologies , Ltd.
1 devices