CORDIS 6 FRENCH 0.062 I.D. PTCA GUIDING CATHTER
K-Number: K915374 · 1992-02-14
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Device Summary
Frequently Asked Questions
What is the CORDIS 6 FRENCH 0.062 I.D. PTCA GUIDING CATHTER?
CORDIS 6 FRENCH 0.062 I.D. PTCA GUIDING CATHTER is a medical device that received FDA 510(k) clearance on 1992-02-14. The listed applicant is Cordis Corp.. The 510(k) number is K915374.
When did CORDIS 6 FRENCH 0.062 I.D. PTCA GUIDING CATHTER receive FDA 510(k) clearance?
CORDIS 6 FRENCH 0.062 I.D. PTCA GUIDING CATHTER received FDA 510(k) clearance on 1992-02-14, under 510(k) number K915374.
Who is the listed applicant for CORDIS 6 FRENCH 0.062 I.D. PTCA GUIDING CATHTER?
The FDA 510(k) record lists Cordis Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CORDIS 6 FRENCH 0.062 I.D. PTCA GUIDING CATHTER?
The FDA product code for CORDIS 6 FRENCH 0.062 I.D. PTCA GUIDING CATHTER is DQY.
Related Clinical Trials
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.
Other records listing Cordis Corp. as applicant
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.
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.
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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