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

FDA 510(k)

DAILIES (NELFILCON A) ONE-DAY

K-Number: K992446 · 1999-08-18

ApplicantCiba Vision Johns Creek Mfg.
Decision Date1999-08-18
Product CodeMVN
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

DAILIES (NELFILCON A) ONE-DAY is the device name listed in this FDA 510(k) record. The listed applicant is Ciba Vision Johns Creek Mfg.. It received FDA 510(k) clearance on 1999-08-18 under 510(k) number K992446. The device is classified under product code MVN. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DAILIES (NELFILCON A) ONE-DAY?

DAILIES (NELFILCON A) ONE-DAY is a medical device that received FDA 510(k) clearance on 1999-08-18. The listed applicant is Ciba Vision Johns Creek Mfg.. The 510(k) number is K992446.

When did DAILIES (NELFILCON A) ONE-DAY receive FDA 510(k) clearance?

DAILIES (NELFILCON A) ONE-DAY received FDA 510(k) clearance on 1999-08-18, under 510(k) number K992446.

Who is the listed applicant for DAILIES (NELFILCON A) ONE-DAY?

The FDA 510(k) record lists Ciba Vision Johns Creek Mfg. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DAILIES (NELFILCON A) ONE-DAY?

The FDA product code for DAILIES (NELFILCON A) ONE-DAY is MVN.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Related Devices (Code: MVN)

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.

K261812HOYA Illumina (sorafilcon A) Daily Disposable Soft Contact Lens; HOYA Illumina (sorafilcon A) Toric Daily Disposable Soft Contact Lens; HOYA Illumina (sorafilcon A) Multifocal Daily Disposable Soft Contact LensHOYA Lamphun , Ltd.K202448DAILIES AquaComfort Plus (DACP) / DACP FreshTech / DACP Toric / DACP MultifocalAlcon Laboratories, Inc.K202036Focus DAILIES / Focus DAILIES Toric / Focus DAILIES Progressives, DAILIES AquaComfort Plus (DACP) / DACP FreshTech / DACP Toric / DACP MultifocalAlcon Laboratories, Inc.K130331SAUFLON CLARITI 1 DAY (SOMOFILCON A) SOFT (HYDROPHILIC) DAILY DISPOSABLE CONTACT LENS WITH UV BLOCKERSauflon Pharmaceuticals, Ltd.K112192NATURELLE DAILY DISPOSABLE (HILAFILCON B) COSMETICALLY TINTED CONTACT LENSBausch & Lomb, Inc.K080632CLEAR1-DAY HIOXIFILCON DAILY DISPOSABLE SOFT CONTACT LENSClearlab SG Pte, Ltd.

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.

↑