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FDA 510(k)

KASIOS TCP

K-Number: K042340 · 2004-11-24

ApplicantKasios Biomaterials
Decision Date2004-11-24
Product CodeMQV
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

KASIOS TCP is the device name listed in this FDA 510(k) record. The listed applicant is Kasios Biomaterials. It received FDA 510(k) clearance on 2004-11-24 under 510(k) number K042340. 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 KASIOS TCP?

KASIOS TCP is a medical device that received FDA 510(k) clearance on 2004-11-24. The listed applicant is Kasios Biomaterials. The 510(k) number is K042340.

When did KASIOS TCP receive FDA 510(k) clearance?

KASIOS TCP received FDA 510(k) clearance on 2004-11-24, under 510(k) number K042340.

Who is the listed applicant for KASIOS TCP?

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

What is the FDA product code for KASIOS TCP?

The FDA product code for KASIOS TCP 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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