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FDA 510(k)

RAPIDO CUT-AWAY GUIDING CATHETER

K-Number: K031505 · 2003-06-25

ApplicantGuidant Corporation
Decision Date2003-06-25
Product CodeDQY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

RAPIDO CUT-AWAY GUIDING CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Guidant Corporation. It received FDA 510(k) clearance on 2003-06-25 under 510(k) number K031505. 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 RAPIDO CUT-AWAY GUIDING CATHETER?

RAPIDO CUT-AWAY GUIDING CATHETER is a medical device that received FDA 510(k) clearance on 2003-06-25. The listed applicant is Guidant Corporation. The 510(k) number is K031505.

When did RAPIDO CUT-AWAY GUIDING CATHETER receive FDA 510(k) clearance?

RAPIDO CUT-AWAY GUIDING CATHETER received FDA 510(k) clearance on 2003-06-25, under 510(k) number K031505.

Who is the listed applicant for RAPIDO CUT-AWAY GUIDING CATHETER?

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

What is the FDA product code for RAPIDO CUT-AWAY GUIDING CATHETER?

The FDA product code for RAPIDO CUT-AWAY GUIDING CATHETER is DQY.

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Other records listing Guidant Corporation as applicant

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Related Devices (Code: DQY)

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.

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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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