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FDA 510(k)

SYNTHACER; SYNTRICER

K-Number: K041177 · 2005-06-23

ApplicantMedartis Medizinprodukte Und Forschung AG
Decision Date2005-06-23
Product CodeMQV
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

SYNTHACER; SYNTRICER is the device name listed in this FDA 510(k) record. The listed applicant is Medartis Medizinprodukte Und Forschung AG. It received FDA 510(k) clearance on 2005-06-23 under 510(k) number K041177. 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 SYNTHACER; SYNTRICER?

SYNTHACER; SYNTRICER is a medical device that received FDA 510(k) clearance on 2005-06-23. The listed applicant is Medartis Medizinprodukte Und Forschung AG. The 510(k) number is K041177.

When did SYNTHACER; SYNTRICER receive FDA 510(k) clearance?

SYNTHACER; SYNTRICER received FDA 510(k) clearance on 2005-06-23, under 510(k) number K041177.

Who is the listed applicant for SYNTHACER; SYNTRICER?

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

What is the FDA product code for SYNTHACER; SYNTRICER?

The FDA product code for SYNTHACER; SYNTRICER is MQV.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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