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FDA 510(k)

RAPIDO CUT-AWAY CUTTER

K-Number: K031459 · 2003-07-23

ApplicantGuidant Corp.
Decision Date2003-07-23
Product CodeDQY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

RAPIDO CUT-AWAY CUTTER is the device name listed in this FDA 510(k) record. The listed applicant is Guidant Corp.. It received FDA 510(k) clearance on 2003-07-23 under 510(k) number K031459. 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 CUTTER?

RAPIDO CUT-AWAY CUTTER is a medical device that received FDA 510(k) clearance on 2003-07-23. The listed applicant is Guidant Corp.. The 510(k) number is K031459.

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

RAPIDO CUT-AWAY CUTTER received FDA 510(k) clearance on 2003-07-23, under 510(k) number K031459.

Who is the listed applicant for RAPIDO CUT-AWAY CUTTER?

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 RAPIDO CUT-AWAY CUTTER?

The FDA product code for RAPIDO CUT-AWAY CUTTER is 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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