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)

BPZ02 MULTIPURPOSE SOLUTION

K-Number: K083757 · 2009-11-18

ApplicantBausch & Lomb, Inc.
Decision Date2009-11-18
Product CodeLYL
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

BPZ02 MULTIPURPOSE SOLUTION is the device name listed in this FDA 510(k) record. The listed applicant is Bausch & Lomb, Inc.. It received FDA 510(k) clearance on 2009-11-18 under 510(k) number K083757. The device is classified under product code LYL. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BPZ02 MULTIPURPOSE SOLUTION?

BPZ02 MULTIPURPOSE SOLUTION is a medical device that received FDA 510(k) clearance on 2009-11-18. The listed applicant is Bausch & Lomb, Inc.. The 510(k) number is K083757.

When did BPZ02 MULTIPURPOSE SOLUTION receive FDA 510(k) clearance?

BPZ02 MULTIPURPOSE SOLUTION received FDA 510(k) clearance on 2009-11-18, under 510(k) number K083757.

Who is the listed applicant for BPZ02 MULTIPURPOSE SOLUTION?

The FDA 510(k) record lists Bausch & Lomb, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BPZ02 MULTIPURPOSE SOLUTION?

The FDA product code for BPZ02 MULTIPURPOSE SOLUTION is LYL.

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 Bausch & Lomb, Inc. 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.

K192005Bausch + Lomb PreVue Inserter for enVista PreloadedK173480Crystalsert Lens Delivery SystemK161012Easy-Load Lens Delivery SystemK131208BAUSCH + LOMB PROCOMFORT (SAMFILCON A) CONTACT LENS, BAUSCH + LOMB PROCOMFORT (SAMFILCON A) CONTACT LENS FOR PRESBYOPIA,K122575BAUSCH & LOMB PUREVISION (BALAFILCON A) VISIBILITY TINTED CONTACT LENS, BAUSCH & LOMB PUREVISION TORIC (BALAFILCON A) VIK113852BAUSCH & LOMB IOL INJECTOR

View all 92 devices →

Related Devices (Code: LYL)

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.

K2113613N Contact Lenses Adjunct CleanerSuzhou 3N Biological Technology Co., Ltd.K210300VueSonic One Contact Lens Cleaning System, VueSonic Advance 2 Contact Lens Cleaning SystemVuesonic, LLCK021699AUTOLENS CLEANING AND DISINFECTING UNITAutolens, Inc.K022687AOSEPT CLEAR CARE CLEANING AND DISINFECTING SOLUTIONCiba Vision CorporationK020802RENUT MULTIPLUS MULLTI-PURPOSE SOLUTIONBausch & Lomb, IncorporatedK994021CONTACLAIR MULTI-PURPOSE CONTACT LENS SOLUTIONStrieter Clinical Research Laboratories, 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.

↑