Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

SMART PERFORMER (Polymacon) Soft (Hydrophilic) Contact Lens

K-Number: K151847 · 2016-03-04

Decision Date2016-03-04
Product CodeLPL
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

SMART PERFORMER (Polymacon) Soft (Hydrophilic) Contact Lens is a medical device manufactured by Smart Performer Corp. , Ltd.. It received FDA 510(k) clearance on 2016-03-04 under approval number K151847. 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 SMART PERFORMER (Polymacon) Soft (Hydrophilic) Contact Lens?

SMART PERFORMER (Polymacon) Soft (Hydrophilic) Contact Lens is a medical device that received FDA 510(k) clearance on 2016-03-04. It is manufactured by Smart Performer Corp. , Ltd.. The 510(k) number is K151847.

When was SMART PERFORMER (Polymacon) Soft (Hydrophilic) Contact Lens approved by the FDA?

SMART PERFORMER (Polymacon) Soft (Hydrophilic) Contact Lens received FDA 510(k) clearance on 2016-03-04, under approval number K151847.

What company makes SMART PERFORMER (Polymacon) Soft (Hydrophilic) Contact Lens?

SMART PERFORMER (Polymacon) Soft (Hydrophilic) Contact Lens is manufactured by Smart Performer Corp. , Ltd..

What is the FDA product code for SMART PERFORMER (Polymacon) Soft (Hydrophilic) Contact Lens?

The FDA product code for SMART PERFORMER (Polymacon) Soft (Hydrophilic) Contact Lens is LPL.

Related Clinical Trials

Other Devices by Smart Performer Corp. , Ltd.

Related Devices (Code: LPL)

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.