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FDA 510(k)

CureOs TCP

K-Number: K191670 · 2020-08-04

Decision Date2020-08-04
Product CodeMQV
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

CureOs TCP is a medical device manufactured by Linacol Muh Dan Kim Cev Tek Med Ith Ihr San VE Tic. It received FDA 510(k) clearance on 2020-08-04 under approval number K191670. 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 CureOs TCP?

CureOs TCP is a medical device that received FDA 510(k) clearance on 2020-08-04. It is manufactured by Linacol Muh Dan Kim Cev Tek Med Ith Ihr San VE Tic. The 510(k) number is K191670.

When was CureOs TCP approved by the FDA?

CureOs TCP received FDA 510(k) clearance on 2020-08-04, under approval number K191670.

What company makes CureOs TCP?

CureOs TCP is manufactured by Linacol Muh Dan Kim Cev Tek Med Ith Ihr San VE Tic.

What is the FDA product code for CureOs TCP?

The FDA product code for CureOs TCP is MQV.

Related Devices (Code: MQV)

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.