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FDA 510(k)

CERASORB ORTHO

K-Number: K014156 · 2002-03-18

ApplicantCurasan AG
Decision Date2002-03-18
Product CodeMQV
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

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 2002-03-18 under 510(k) number K014156. 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 ORTHO?

CERASORB ORTHO is a medical device that received FDA 510(k) clearance on 2002-03-18. The listed applicant is Curasan AG. The 510(k) number is K014156.

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

CERASORB ORTHO received FDA 510(k) clearance on 2002-03-18, under 510(k) number K014156.

Who is the listed applicant for 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 CERASORB ORTHO?

The FDA product code for 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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