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FDA 510(k)

Alians Fragment Specific

K-Number: K170843 · 2017-06-16

Decision Date2017-06-16
Product CodeHRS
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Alians Fragment Specific is a medical device manufactured by Newclip Technics. It received FDA 510(k) clearance on 2017-06-16 under approval number K170843. The device is classified under product code HRS. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Alians Fragment Specific?

Alians Fragment Specific is a medical device that received FDA 510(k) clearance on 2017-06-16. It is manufactured by Newclip Technics. The 510(k) number is K170843.

When was Alians Fragment Specific approved by the FDA?

Alians Fragment Specific received FDA 510(k) clearance on 2017-06-16, under approval number K170843.

What company makes Alians Fragment Specific?

Alians Fragment Specific is manufactured by Newclip Technics.

What is the FDA product code for Alians Fragment Specific?

The FDA product code for Alians Fragment Specific is HRS.

Other Devices by Newclip Technics

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Related Devices (Code: HRS)

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.