Castor, Achilles and Hermes NC PTA Balloon Dilatation Catheter
K-Number: K160941 · 2016-12-13
Device Summary
Frequently Asked Questions
What is the Castor, Achilles and Hermes NC PTA Balloon Dilatation Catheter?
Castor, Achilles and Hermes NC PTA Balloon Dilatation Catheter is a medical device that received FDA 510(k) clearance on 2016-12-13. The listed applicant is Brosmed Medical Co., Ltd.. The 510(k) number is K160941.
When did Castor, Achilles and Hermes NC PTA Balloon Dilatation Catheter receive FDA 510(k) clearance?
Castor, Achilles and Hermes NC PTA Balloon Dilatation Catheter received FDA 510(k) clearance on 2016-12-13, under 510(k) number K160941.
Who is the listed applicant for Castor, Achilles and Hermes NC PTA Balloon Dilatation Catheter?
The FDA 510(k) record lists Brosmed Medical Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Castor, Achilles and Hermes NC PTA Balloon Dilatation Catheter?
The FDA product code for Castor, Achilles and Hermes NC PTA Balloon Dilatation Catheter is LIT.
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 Brosmed Medical Co., Ltd. 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: LIT)
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.