FDA 510(k)

SmartTarget

K-Number: K170250 · 2017-06-07

Decision Date2017-06-07

Product CodeLLZ

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

SmartTarget is the device name listed in this FDA 510(k) record. The listed applicant is Smarttarget, Ltd.. It received FDA 510(k) clearance on 2017-06-07 under 510(k) number K170250. 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 SmartTarget?

SmartTarget is a medical device that received FDA 510(k) clearance on 2017-06-07. The listed applicant is Smarttarget, Ltd.. The 510(k) number is K170250.

When did SmartTarget receive FDA 510(k) clearance?

SmartTarget received FDA 510(k) clearance on 2017-06-07, under 510(k) number K170250.

Who is the listed applicant for SmartTarget?

The FDA 510(k) record lists Smarttarget, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SmartTarget?

The FDA product code for SmartTarget is LLZ.

Related Devices (Code: LLZ)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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.