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FDA 510(k)

BloodSTOP iX Battle Matrix

K-Number: K160130 · 2016-06-29

ApplicantLifescience Plus, Inc.
Decision Date2016-06-29
Product CodeQSY
DecisionSubstantially Equivalent

Device Summary

BloodSTOP iX Battle Matrix is a medical device manufactured by Lifescience Plus, Inc.. It received FDA 510(k) clearance on 2016-06-29 under approval number K160130. The device is classified under product code QSY. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BloodSTOP iX Battle Matrix?

BloodSTOP iX Battle Matrix is a medical device that received FDA 510(k) clearance on 2016-06-29. It is manufactured by Lifescience Plus, Inc.. The 510(k) number is K160130.

When was BloodSTOP iX Battle Matrix approved by the FDA?

BloodSTOP iX Battle Matrix received FDA 510(k) clearance on 2016-06-29, under approval number K160130.

What company makes BloodSTOP iX Battle Matrix?

BloodSTOP iX Battle Matrix is manufactured by Lifescience Plus, Inc..

What is the FDA product code for BloodSTOP iX Battle Matrix?

The FDA product code for BloodSTOP iX Battle Matrix is QSY.

Other Devices by Lifescience Plus, Inc.

K253017BloodSTOP iX Trauma Matrix (TM-iX-20)

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Official Source

View on FDA Database →

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

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