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FDA 510(k)

COR DOT CMV

K-Number: K853989 · 1986-06-13

ApplicantCordis Corp.
Decision Date1986-06-13
Product CodeGQI
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

COR DOT CMV is the device name listed in this FDA 510(k) record. The listed applicant is Cordis Corp.. It received FDA 510(k) clearance on 1986-06-13 under 510(k) number K853989. The device is classified under product code GQI. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COR DOT CMV?

COR DOT CMV is a medical device that received FDA 510(k) clearance on 1986-06-13. The listed applicant is Cordis Corp.. The 510(k) number is K853989.

When did COR DOT CMV receive FDA 510(k) clearance?

COR DOT CMV received FDA 510(k) clearance on 1986-06-13, under 510(k) number K853989.

Who is the listed applicant for COR DOT CMV?

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 COR DOT CMV?

The FDA product code for COR DOT CMV is GQI.

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.

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Related Devices (Code: GQI)

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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