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FDA 510(k)

VANTAGE PERIPHERAL DILATATION CATHETER

K-Number: K965183 · 1997-04-24

ApplicantGuidant Corp.
Decision Date1997-04-24
Product CodeLIT
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

VANTAGE PERIPHERAL DILATATION CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Guidant Corp.. It received FDA 510(k) clearance on 1997-04-24 under 510(k) number K965183. The device is classified under product code LIT. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VANTAGE PERIPHERAL DILATATION CATHETER?

VANTAGE PERIPHERAL DILATATION CATHETER is a medical device that received FDA 510(k) clearance on 1997-04-24. The listed applicant is Guidant Corp.. The 510(k) number is K965183.

When did VANTAGE PERIPHERAL DILATATION CATHETER receive FDA 510(k) clearance?

VANTAGE PERIPHERAL DILATATION CATHETER received FDA 510(k) clearance on 1997-04-24, under 510(k) number K965183.

Who is the listed applicant for VANTAGE PERIPHERAL DILATATION CATHETER?

The FDA 510(k) record lists Guidant Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VANTAGE PERIPHERAL DILATATION CATHETER?

The FDA product code for VANTAGE PERIPHERAL DILATATION CATHETER is LIT.

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Related Devices (Code: LIT)

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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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