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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 the device name listed in this FDA 510(k) record. The listed applicant is Smart Performer Corp. , Ltd.. It received FDA 510(k) clearance on 2016-03-04 under 510(k) 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. The listed applicant is Smart Performer Corp. , Ltd.. The 510(k) number is K151847.

When did SMART PERFORMER (Polymacon) Soft (Hydrophilic) Contact Lens receive FDA 510(k) clearance?

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

Who is the listed applicant for SMART PERFORMER (Polymacon) Soft (Hydrophilic) Contact Lens?

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

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

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.

Other records listing Smart Performer Corp. , Ltd. as applicant

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.

Related Devices (Code: LPL)

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.

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.