CONQUEST 40 PTA DILATATION CATHETER
K-Number: K120660 · 2012-03-15
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Device Summary
Frequently Asked Questions
What is the CONQUEST 40 PTA DILATATION CATHETER?
CONQUEST 40 PTA DILATATION CATHETER is a medical device that received FDA 510(k) clearance on 2012-03-15. The listed applicant is Bard Peripheral Vascular, Inc.. The 510(k) number is K120660.
When did CONQUEST 40 PTA DILATATION CATHETER receive FDA 510(k) clearance?
CONQUEST 40 PTA DILATATION CATHETER received FDA 510(k) clearance on 2012-03-15, under 510(k) number K120660.
Who is the listed applicant for CONQUEST 40 PTA DILATATION CATHETER?
The FDA 510(k) record lists Bard Peripheral Vascular, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CONQUEST 40 PTA DILATATION CATHETER?
The FDA product code for CONQUEST 40 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 Bard Peripheral Vascular, 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.
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