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FDA 510(k)

Neocis Guidance System

K-Number: K182776 · 2018-12-21

ApplicantNeocis, Inc.
Decision Date2018-12-21
Product CodePLV
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

Neocis Guidance System is a medical device manufactured by Neocis, Inc.. It received FDA 510(k) clearance on 2018-12-21 under approval number K182776. The device is classified under product code PLV. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Neocis Guidance System?

Neocis Guidance System is a medical device that received FDA 510(k) clearance on 2018-12-21. It is manufactured by Neocis, Inc.. The 510(k) number is K182776.

When was Neocis Guidance System approved by the FDA?

Neocis Guidance System received FDA 510(k) clearance on 2018-12-21, under approval number K182776.

What company makes Neocis Guidance System?

Neocis Guidance System is manufactured by Neocis, Inc..

What is the FDA product code for Neocis Guidance System?

The FDA product code for Neocis Guidance System is PLV.

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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.