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FDA 510(k)

AmCAD-UV

K-Number: K170069 · 2017-04-26

ApplicantAmcad Biomed Corporation
Decision Date2017-04-26
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

AmCAD-UV is a medical device manufactured by Amcad Biomed Corporation. It received FDA 510(k) clearance on 2017-04-26 under approval number K170069. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AmCAD-UV?

AmCAD-UV is a medical device that received FDA 510(k) clearance on 2017-04-26. It is manufactured by Amcad Biomed Corporation. The 510(k) number is K170069.

When was AmCAD-UV approved by the FDA?

AmCAD-UV received FDA 510(k) clearance on 2017-04-26, under approval number K170069.

What company makes AmCAD-UV?

AmCAD-UV is manufactured by Amcad Biomed Corporation.

What is the FDA product code for AmCAD-UV?

The FDA product code for AmCAD-UV is LLZ.

Other Devices by Amcad Biomed Corporation

K162574AmCAD-US K180867AmCAD-UO K180006AmCAD-UT Detection 2.2 K203555AmCAD-UT

Related Devices (Code: LLZ)

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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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