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FDA 510(k)

CERASORB M ORTHO

K-Number: K040216 · 2004-03-26

ApplicantCurasan AG
Decision Date2004-03-26
Product CodeMQV
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

CERASORB M ORTHO is the device name listed in this FDA 510(k) record. The listed applicant is Curasan AG. It received FDA 510(k) clearance on 2004-03-26 under 510(k) number K040216. The device is classified under product code MQV. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CERASORB M ORTHO?

CERASORB M ORTHO is a medical device that received FDA 510(k) clearance on 2004-03-26. The listed applicant is Curasan AG. The 510(k) number is K040216.

When did CERASORB M ORTHO receive FDA 510(k) clearance?

CERASORB M ORTHO received FDA 510(k) clearance on 2004-03-26, under 510(k) number K040216.

Who is the listed applicant for CERASORB M ORTHO?

The FDA 510(k) record lists Curasan AG as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CERASORB M ORTHO?

The FDA product code for CERASORB M ORTHO is MQV.

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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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