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FDA 510(k)

CORDIS PTCA GUIDING CATHETER, MODIFICATION

K-Number: K913783 · 1991-10-18

ApplicantDow Corning Wright
Decision Date1991-10-18
Product CodeDQY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CORDIS PTCA GUIDING CATHETER, MODIFICATION is the device name listed in this FDA 510(k) record. The listed applicant is Dow Corning Wright. It received FDA 510(k) clearance on 1991-10-18 under 510(k) number K913783. 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 CORDIS PTCA GUIDING CATHETER, MODIFICATION?

CORDIS PTCA GUIDING CATHETER, MODIFICATION is a medical device that received FDA 510(k) clearance on 1991-10-18. The listed applicant is Dow Corning Wright. The 510(k) number is K913783.

When did CORDIS PTCA GUIDING CATHETER, MODIFICATION receive FDA 510(k) clearance?

CORDIS PTCA GUIDING CATHETER, MODIFICATION received FDA 510(k) clearance on 1991-10-18, under 510(k) number K913783.

Who is the listed applicant for CORDIS PTCA GUIDING CATHETER, MODIFICATION?

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

What is the FDA product code for CORDIS PTCA GUIDING CATHETER, MODIFICATION?

The FDA product code for CORDIS PTCA GUIDING CATHETER, MODIFICATION is DQY.

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Other records listing Dow Corning Wright 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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