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FDA 510(k)

CORIX 70 PLUS-USV

K-Number: K031802 · 2003-07-21

ApplicantCoramex, S.A.
Decision Date2003-07-21
Product CodeEHD
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

CORIX 70 PLUS-USV is the device name listed in this FDA 510(k) record. The listed applicant is Coramex, S.A.. It received FDA 510(k) clearance on 2003-07-21 under 510(k) number K031802. The device is classified under product code EHD. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CORIX 70 PLUS-USV?

CORIX 70 PLUS-USV is a medical device that received FDA 510(k) clearance on 2003-07-21. The listed applicant is Coramex, S.A.. The 510(k) number is K031802.

When did CORIX 70 PLUS-USV receive FDA 510(k) clearance?

CORIX 70 PLUS-USV received FDA 510(k) clearance on 2003-07-21, under 510(k) number K031802.

Who is the listed applicant for CORIX 70 PLUS-USV?

The FDA 510(k) record lists Coramex, S.A. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CORIX 70 PLUS-USV?

The FDA product code for CORIX 70 PLUS-USV is EHD.

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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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