FDA 510(k)

VENTURI MiNO TG600/14

K-Number: K143004 · 2016-01-05

Decision Date2016-01-05

Product CodeOMP

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

VENTURI MiNO TG600/14 is a medical device manufactured by Talley Group, Ltd.. It received FDA 510(k) clearance on 2016-01-05 under approval number K143004. The device is classified under product code OMP. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VENTURI MiNO TG600/14?

VENTURI MiNO TG600/14 is a medical device that received FDA 510(k) clearance on 2016-01-05. It is manufactured by Talley Group, Ltd.. The 510(k) number is K143004.

When was VENTURI MiNO TG600/14 approved by the FDA?

VENTURI MiNO TG600/14 received FDA 510(k) clearance on 2016-01-05, under approval number K143004.

What company makes VENTURI MiNO TG600/14?

VENTURI MiNO TG600/14 is manufactured by Talley Group, Ltd..

What is the FDA product code for VENTURI MiNO TG600/14?

The FDA product code for VENTURI MiNO TG600/14 is OMP.

Other Devices by Talley Group, Ltd.

K151263Venturi Gauze Wound Care Sets with Portal Drain

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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.