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FDA 510(k)

SIGHT SAVER ALL PURPOSE LENS CARRYING CASE

K-Number: K852384 · 1985-07-31

ApplicantBausch & Lomb, Inc.
Decision Date1985-07-31
Product CodeHPX
DecisionSubstantially Equivalent

Device Summary

SIGHT SAVER ALL PURPOSE LENS CARRYING CASE 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 1985-07-31 under 510(k) number K852384. The device is classified under product code HPX. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SIGHT SAVER ALL PURPOSE LENS CARRYING CASE?

SIGHT SAVER ALL PURPOSE LENS CARRYING CASE is a medical device that received FDA 510(k) clearance on 1985-07-31. The listed applicant is Bausch & Lomb, Inc.. The 510(k) number is K852384.

When did SIGHT SAVER ALL PURPOSE LENS CARRYING CASE receive FDA 510(k) clearance?

SIGHT SAVER ALL PURPOSE LENS CARRYING CASE received FDA 510(k) clearance on 1985-07-31, under 510(k) number K852384.

Who is the listed applicant for SIGHT SAVER ALL PURPOSE LENS CARRYING CASE?

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 SIGHT SAVER ALL PURPOSE LENS CARRYING CASE?

The FDA product code for SIGHT SAVER ALL PURPOSE LENS CARRYING CASE 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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