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FDA 510(k)

Precision1

K-Number: K182902 · 2018-12-11

ApplicantAlcon Laboratories, Inc.
Decision Date2018-12-11
Product CodeLPL
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

Precision1 is a medical device manufactured by Alcon Laboratories, Inc.. It received FDA 510(k) clearance on 2018-12-11 under approval number K182902. The device is classified under product code LPL. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Precision1?

Precision1 is a medical device that received FDA 510(k) clearance on 2018-12-11. It is manufactured by Alcon Laboratories, Inc.. The 510(k) number is K182902.

When was Precision1 approved by the FDA?

Precision1 received FDA 510(k) clearance on 2018-12-11, under approval number K182902.

What company makes Precision1?

Precision1 is manufactured by Alcon Laboratories, Inc..

What is the FDA product code for Precision1?

The FDA product code for Precision1 is LPL.

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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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