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)

AQUIFY MULTI-PURPOSE SOLUTION

K-Number: K033608 · 2004-02-02

ApplicantCiba Vision Corporation
Decision Date2004-02-02
Product CodeLPN
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

AQUIFY MULTI-PURPOSE SOLUTION is the device name listed in this FDA 510(k) record. The listed applicant is Ciba Vision Corporation. It received FDA 510(k) clearance on 2004-02-02 under 510(k) number K033608. The device is classified under product code LPN. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AQUIFY MULTI-PURPOSE SOLUTION?

AQUIFY MULTI-PURPOSE SOLUTION is a medical device that received FDA 510(k) clearance on 2004-02-02. The listed applicant is Ciba Vision Corporation. The 510(k) number is K033608.

When did AQUIFY MULTI-PURPOSE SOLUTION receive FDA 510(k) clearance?

AQUIFY MULTI-PURPOSE SOLUTION received FDA 510(k) clearance on 2004-02-02, under 510(k) number K033608.

Who is the listed applicant for AQUIFY MULTI-PURPOSE SOLUTION?

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

What is the FDA product code for AQUIFY MULTI-PURPOSE SOLUTION?

The FDA product code for AQUIFY MULTI-PURPOSE SOLUTION is LPN.

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

Other records listing Ciba Vision Corporation 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.

K123994DAILIES AQUACOMFORT PLUS, DAILIES AQUACOMFORT PLUS TORIC, DAILIES AQUACOMFORT PLUS MULTIFOCALK113168DAILIES TOTAL DALIES TOTAL FOR ASTIGMATISM DAILIES TOTAL MULTIFOCAL DAILIES TOTAL MULTIFOCAL TORICK083216CIBA VISION (NELFILCON A) ONE-DAY SOFT CONTACT LENSESK073459CIBA VISION (LOTRAFILCON B) SOFT CONTACT LENSESK072777CIBA VISION (NELFILCON A) ONE-DAY SOFT CONTACT LENSESK062262CIBA VISION (SIFILCON A) SPHERICAL, TORIC, MULTIFOCAL AND MULTIFOCAL TORIC DESIGNS

View all 43 devices →

Related Devices (Code: LPN)

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.

K253795MeniSept 3% Hydrogen Peroxide Cleaning & Disinfecting SolutionMenicon Co, Ltd.K222541Bausch + Lomb Preservative Free Lubricating and Rewetting DropsBausch & Lomb, IncorporatedK221263Aqua Naina Plus Sterile Saline SolutionChemtex USA, Inc.K202932ABT12 multi-purpose solutionBausch & Lomb, IncorporatedK210051OTE MPS 045 Multi-purpose Lens Care SolutionOte North America, LLCK193441Aqua Naina Sterile Saline SolutionChemtex USA, Inc.

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.

↑