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FDA 510(k)

ACS VIKING GUIDING CATHETER

K-Number: K972484 · 1997-09-26

ApplicantGuidant Corp.
Decision Date1997-09-26
Product CodeDQY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ACS VIKING 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 1997-09-26 under 510(k) number K972484. 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 ACS VIKING GUIDING CATHETER?

ACS VIKING GUIDING CATHETER is a medical device that received FDA 510(k) clearance on 1997-09-26. The listed applicant is Guidant Corp.. The 510(k) number is K972484.

When did ACS VIKING GUIDING CATHETER receive FDA 510(k) clearance?

ACS VIKING GUIDING CATHETER received FDA 510(k) clearance on 1997-09-26, under 510(k) number K972484.

Who is the listed applicant for ACS VIKING 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 ACS VIKING GUIDING CATHETER?

The FDA product code for ACS VIKING GUIDING CATHETER is DQY.

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Other records listing Guidant Corp. as applicant

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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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