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. The listed applicant is Thrombolex, Inc.. The 510(k) number is K192598.
When did Bashir S-B Endovascular Catheter, Ref. No. 7101 receive FDA 510(k) clearance?
Bashir S-B Endovascular Catheter, Ref. No. 7101 received FDA 510(k) clearance on 2019-10-18, under 510(k) number K192598.
Who is the listed applicant for Bashir S-B Endovascular Catheter, Ref. No. 7101?
The FDA 510(k) record lists Thrombolex, Inc. as the applicant. This does not by itself establish the device manufacturer.
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
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.
Other records listing Thrombolex, Inc. 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: QEY)
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.