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FDA 510(k)

329 CORDIS ENCOR PREVENOUS ARTRIAL & VENTRICULAR

K-Number: K852253 · 1985-07-29

ApplicantCordis Corp.
Decision Date1985-07-29
Product CodeDTD
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

329 CORDIS ENCOR PREVENOUS ARTRIAL & VENTRICULAR is the device name listed in this FDA 510(k) record. The listed applicant is Cordis Corp.. It received FDA 510(k) clearance on 1985-07-29 under 510(k) number K852253. The device is classified under product code DTD. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 329 CORDIS ENCOR PREVENOUS ARTRIAL & VENTRICULAR?

329 CORDIS ENCOR PREVENOUS ARTRIAL & VENTRICULAR is a medical device that received FDA 510(k) clearance on 1985-07-29. The listed applicant is Cordis Corp.. The 510(k) number is K852253.

When did 329 CORDIS ENCOR PREVENOUS ARTRIAL & VENTRICULAR receive FDA 510(k) clearance?

329 CORDIS ENCOR PREVENOUS ARTRIAL & VENTRICULAR received FDA 510(k) clearance on 1985-07-29, under 510(k) number K852253.

Who is the listed applicant for 329 CORDIS ENCOR PREVENOUS ARTRIAL & VENTRICULAR?

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 329 CORDIS ENCOR PREVENOUS ARTRIAL & VENTRICULAR?

The FDA product code for 329 CORDIS ENCOR PREVENOUS ARTRIAL & VENTRICULAR is DTD.

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Other records listing Cordis Corp. as applicant

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Related Devices (Code: DTD)

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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