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FDA 510(k)

CORDIA NP

K-Number: K800992 · 1980-05-08

ApplicantCordis Corp.
Decision Date1980-05-08
Product CodeDHC
Advisory CommitteeIM
DecisionSubstantially Equivalent

Device Summary

CORDIA NP is the device name listed in this FDA 510(k) record. The listed applicant is Cordis Corp.. It received FDA 510(k) clearance on 1980-05-08 under 510(k) number K800992. The device is classified under product code DHC. It was reviewed by the IM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CORDIA NP?

CORDIA NP is a medical device that received FDA 510(k) clearance on 1980-05-08. The listed applicant is Cordis Corp.. The 510(k) number is K800992.

When did CORDIA NP receive FDA 510(k) clearance?

CORDIA NP received FDA 510(k) clearance on 1980-05-08, under 510(k) number K800992.

Who is the listed applicant for CORDIA NP?

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 CORDIA NP?

The FDA product code for CORDIA NP is DHC.

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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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