Atlas Gold PTA Dilatation Catheter
K-Number: K181323 · 2018-08-03
Device Summary
Frequently Asked Questions
What is the Atlas Gold PTA Dilatation Catheter?
Atlas Gold PTA Dilatation Catheter is a medical device that received FDA 510(k) clearance on 2018-08-03. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K181323.
When did Atlas Gold PTA Dilatation Catheter receive FDA 510(k) clearance?
Atlas Gold PTA Dilatation Catheter received FDA 510(k) clearance on 2018-08-03, under 510(k) number K181323.
Who is the listed applicant for Atlas Gold PTA Dilatation Catheter?
The FDA 510(k) record lists C.R. Bard, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Atlas Gold PTA Dilatation Catheter?
The FDA product code for Atlas Gold PTA 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 C.R. Bard, 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: 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.