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FDA 510(k)

BAUSCH & LOMB STERILE ALL PURPOSE SOLU

K-Number: K820511 · 1982-04-09

ApplicantBausch & Lomb, Inc.
Decision Date1982-04-09
Product CodeHPX
DecisionSubstantially Equivalent

Device Summary

BAUSCH & LOMB STERILE ALL PURPOSE SOLU 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 1982-04-09 under 510(k) number K820511. The device is classified under product code HPX. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BAUSCH & LOMB STERILE ALL PURPOSE SOLU?

BAUSCH & LOMB STERILE ALL PURPOSE SOLU is a medical device that received FDA 510(k) clearance on 1982-04-09. The listed applicant is Bausch & Lomb, Inc.. The 510(k) number is K820511.

When did BAUSCH & LOMB STERILE ALL PURPOSE SOLU receive FDA 510(k) clearance?

BAUSCH & LOMB STERILE ALL PURPOSE SOLU received FDA 510(k) clearance on 1982-04-09, under 510(k) number K820511.

Who is the listed applicant for BAUSCH & LOMB STERILE ALL PURPOSE SOLU?

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 BAUSCH & LOMB STERILE ALL PURPOSE SOLU?

The FDA product code for BAUSCH & LOMB STERILE ALL PURPOSE SOLU is HPX.

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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

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Related Devices (Code: HPX)

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.

K955777PMMA CLASICRand Scientific Corp.K940106KERATOPLASTY SUTURING LENSVisionary Technologies of Miami, Inc.K913081MULTI-VIEW BIFOCALSCamp Contact LensesK897021MARTIN-HENSLEY SEGMENT LENSBruce W. Martin O.D. and Edward HensleyK895411OPTIKEM PMMA CONTACT LENSOptikem Polymers, Inc.K874591ILLUMINATING INFUSION CONTACT LENS FOR EYE SURGERYVitreo Dynamics, Co.

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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