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FDA 510(k)

MODIFICATION TO CERASORB ORTHO

K-Number: K031651 · 2003-08-13

ApplicantCurasan AG
Decision Date2003-08-13
Product CodeMQV
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

MODIFICATION TO CERASORB 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 2003-08-13 under 510(k) number K031651. 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 MODIFICATION TO CERASORB ORTHO?

MODIFICATION TO CERASORB ORTHO is a medical device that received FDA 510(k) clearance on 2003-08-13. The listed applicant is Curasan AG. The 510(k) number is K031651.

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

MODIFICATION TO CERASORB ORTHO received FDA 510(k) clearance on 2003-08-13, under 510(k) number K031651.

Who is the listed applicant for MODIFICATION TO CERASORB 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 MODIFICATION TO CERASORB ORTHO?

The FDA product code for MODIFICATION TO CERASORB 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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