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FDA 510(k)

T-32;T-40;T-44;T-52;T-72;TT-50

K-Number: K152412 · 2016-04-29

Decision Date2016-04-29
Product CodeLEJ
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

T-32;T-40;T-44;T-52;T-72;TT-50 is a medical device manufactured by Tanses Technologies, Inc.. It received FDA 510(k) clearance on 2016-04-29 under approval number K152412. The device is classified under product code LEJ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the T-32;T-40;T-44;T-52;T-72;TT-50?

T-32;T-40;T-44;T-52;T-72;TT-50 is a medical device that received FDA 510(k) clearance on 2016-04-29. It is manufactured by Tanses Technologies, Inc.. The 510(k) number is K152412.

When was T-32;T-40;T-44;T-52;T-72;TT-50 approved by the FDA?

T-32;T-40;T-44;T-52;T-72;TT-50 received FDA 510(k) clearance on 2016-04-29, under approval number K152412.

What company makes T-32;T-40;T-44;T-52;T-72;TT-50?

T-32;T-40;T-44;T-52;T-72;TT-50 is manufactured by Tanses Technologies, Inc..

What is the FDA product code for T-32;T-40;T-44;T-52;T-72;TT-50?

The FDA product code for T-32;T-40;T-44;T-52;T-72;TT-50 is LEJ.

Other Devices by Tanses Technologies, Inc.

Related Devices (Code: LEJ)

Official Source

View on FDA Database →

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