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FDA 510(k)

5F GUIDING CATHETER

K-Number: K000598 · 2000-03-24

ApplicantGuidant Corp.
Decision Date2000-03-24
Product CodeDQY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

5F GUIDING 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 2000-03-24 under 510(k) number K000598. The device is classified under product code DQY. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 5F GUIDING CATHETER?

5F GUIDING CATHETER is a medical device that received FDA 510(k) clearance on 2000-03-24. The listed applicant is Guidant Corp.. The 510(k) number is K000598.

When did 5F GUIDING CATHETER receive FDA 510(k) clearance?

5F GUIDING CATHETER received FDA 510(k) clearance on 2000-03-24, under 510(k) number K000598.

Who is the listed applicant for 5F GUIDING 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 5F GUIDING CATHETER?

The FDA product code for 5F GUIDING CATHETER is DQY.

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Other records listing Guidant Corp. as applicant

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Related Devices (Code: DQY)

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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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