FDA PMA

Fluid, intraocular

PMA Number: P910071 · 2025-12-22

ApplicantBausch & Lomb

Decision Date2025-12-22

PMA NumberP910071

Product CodeLWL

Device ClassClass 3

Medical SpecialtyO

Regulation Number21 CFR 8

Advisory CommitteeOP

Device Summary

Fluid, intraocular is the device name listed in this FDA 510(k) record. The listed applicant is Bausch & Lomb. It received FDA 510(k) clearance on 2025-12-22. The device is classified under product code LWL. It was reviewed by the OP advisory panel.

Frequently Asked Questions

What is the Fluid, intraocular?

Fluid, intraocular is a medical device that received FDA 510(k) clearance on 2025-12-22. The listed applicant is Bausch & Lomb.

When did Fluid, intraocular receive FDA 510(k) clearance?

The clearance date for Fluid, intraocular can be found in the official FDA records.

Who is the listed applicant for Fluid, intraocular?

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

What is the FDA product code for Fluid, intraocular?

The FDA product code for Fluid, intraocular is LWL.

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_RECRUITING NCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITING NCT04745156A Study Using Brain Stimulation and Behavioral Therapy to Increase Extent of Resection in Low-Grade GliomasNOT_YET_RECRUITING NCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDED

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.