Bashir S-B Endovascular Catheter, Ref. No. 7101
K-Number: K192598 · 2019-10-18
Device Summary
Frequently Asked Questions
What is the Bashir S-B Endovascular Catheter, Ref. No. 7101?
Bashir S-B Endovascular Catheter, Ref. No. 7101 is a medical device that received FDA 510(k) clearance on 2019-10-18. It is manufactured by Thrombolex, Inc.. The 510(k) number is K192598.
When was Bashir S-B Endovascular Catheter, Ref. No. 7101 approved by the FDA?
Bashir S-B Endovascular Catheter, Ref. No. 7101 received FDA 510(k) clearance on 2019-10-18, under approval number K192598.
What company makes Bashir S-B Endovascular Catheter, Ref. No. 7101?
Bashir S-B Endovascular Catheter, Ref. No. 7101 is manufactured by Thrombolex, Inc..
What is the FDA product code for Bashir S-B Endovascular Catheter, Ref. No. 7101?
The FDA product code for Bashir S-B Endovascular Catheter, Ref. No. 7101 is QEY.
Related Clinical Trials
Other Devices by Thrombolex, Inc.
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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.