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FDA 510(k)

Bashir S-B Endovascular Catheter, Ref. No. 7101

K-Number: K192598 · 2019-10-18

Decision Date2019-10-18
Product CodeQEY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Bashir S-B Endovascular Catheter, Ref. No. 7101 is a medical device manufactured by Thrombolex, Inc.. It received FDA 510(k) clearance on 2019-10-18 under approval number K192598. The device is classified under product code QEY. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

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

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