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FDA 510(k)

BAUSCH & LOMB FREQUENT REPLACEMENT CASE SYSTEM

K-Number: K896685 · 1989-12-26

ApplicantBausch & Lomb, Inc.
Decision Date1989-12-26
Product CodeLRX
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

BAUSCH & LOMB FREQUENT REPLACEMENT CASE SYSTEM 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 1989-12-26 under 510(k) number K896685. The device is classified under product code LRX. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BAUSCH & LOMB FREQUENT REPLACEMENT CASE SYSTEM?

BAUSCH & LOMB FREQUENT REPLACEMENT CASE SYSTEM is a medical device that received FDA 510(k) clearance on 1989-12-26. The listed applicant is Bausch & Lomb, Inc.. The 510(k) number is K896685.

When did BAUSCH & LOMB FREQUENT REPLACEMENT CASE SYSTEM receive FDA 510(k) clearance?

BAUSCH & LOMB FREQUENT REPLACEMENT CASE SYSTEM received FDA 510(k) clearance on 1989-12-26, under 510(k) number K896685.

Who is the listed applicant for BAUSCH & LOMB FREQUENT REPLACEMENT CASE SYSTEM?

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 FREQUENT REPLACEMENT CASE SYSTEM?

The FDA product code for BAUSCH & LOMB FREQUENT REPLACEMENT CASE SYSTEM is LRX.

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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: LRX)

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.

K252175LANDR Contact LENS CaseFourth Axis, LLCK250495MINI VP1 (PL67_F); MINI VP1 (PL61_F)Avizor S.A.K240095CAREUS Contact Lens Case (Model 1, Model 2, Model 3, Model 4, Model 5, Model 6)Shanghai Care US Medical Product Co., Ltd.K231123Phoenix Contact Lens Case - dome top flat pack (CL-01); Phoenix Contact Lens Case - classic flat pack (CL-02); Phoenix Contact Lens Case - sunglass shape flat pack (CL-03)Phoenix Innovative Healthcare Manufacturers Pvt. , Ltd.K173538Clear Care Cleaning & Disinfecting Solution, AOCup Lens Case with AODiscAlcon Laboratories, Inc.K172925Contact Lens Case, Model: A-1, B-1P L Overseas Limited

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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