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FDA 510(k)

Menicon Progent Protein Remover for Rigid Gas Permeable Contact Lenses

K-Number: K173136 · 2017-11-16

ApplicantMenicon Co, Ltd.
Decision Date2017-11-16
Product CodeMRC
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

Menicon Progent Protein Remover for Rigid Gas Permeable Contact Lenses is a medical device manufactured by Menicon Co, Ltd.. It received FDA 510(k) clearance on 2017-11-16 under approval number K173136. The device is classified under product code MRC. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Menicon Progent Protein Remover for Rigid Gas Permeable Contact Lenses?

Menicon Progent Protein Remover for Rigid Gas Permeable Contact Lenses is a medical device that received FDA 510(k) clearance on 2017-11-16. It is manufactured by Menicon Co, Ltd.. The 510(k) number is K173136.

When was Menicon Progent Protein Remover for Rigid Gas Permeable Contact Lenses approved by the FDA?

Menicon Progent Protein Remover for Rigid Gas Permeable Contact Lenses received FDA 510(k) clearance on 2017-11-16, under approval number K173136.

What company makes Menicon Progent Protein Remover for Rigid Gas Permeable Contact Lenses?

Menicon Progent Protein Remover for Rigid Gas Permeable Contact Lenses is manufactured by Menicon Co, Ltd..

What is the FDA product code for Menicon Progent Protein Remover for Rigid Gas Permeable Contact Lenses?

The FDA product code for Menicon Progent Protein Remover for Rigid Gas Permeable Contact Lenses is MRC.

Related Clinical Trials

NCT06864858 Clinical Evaluation of Two Cosmetic Contact Lenses COMPLETED NCT07566234 Evaluation of Contact Lenses and Myopia. NOT_YET_RECRUITING NCT07600645 Contact Lens Trial Fitting Experience NOT_YET_RECRUITING NCT06749496 Evaluation of Delefilcon A and Senofilcon A Daily Disposable Toric Soft Contact Lenses Over One Week of Wear COMPLETED NCT07557147 Single-arm, Multi-center Study Evaluating the Acceptance and Feasibility of a Digital Remote Monitoring Tool Configured for Patients With ATTR-CM: ACO-Monitor NOT_YET_RECRUITING NCT07586982 Clinical Performance of Verofilcon A Toric Contact Lenses RECRUITING

Other Devices by Menicon Co, Ltd.

K180819One Day Flat Pack (hioxifilcon A) Daily Disposable Soft Contact Lens K180004Menicon ASRB (asmofilcon A) Silicone Hydrogel Soft Contact Lens K193399Miru 1day UpSide (midafilcon A) K191872Menicon 3% Hydrogen Peroxide Cleaning and Disinfecting Solution PMA P990018Lens, contact, orthokeratology, overnight

Related Devices (Code: MRC)

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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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