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FDA 510(k)

ITEM #352/#CS352* CONTACT LENS CASES

K-Number: K890533 · 1989-06-23

ApplicantMagnivision, Inc.
Decision Date1989-06-23
Product CodeLRX
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

ITEM #352/#CS352* CONTACT LENS CASES is the device name listed in this FDA 510(k) record. The listed applicant is Magnivision, Inc.. It received FDA 510(k) clearance on 1989-06-23 under 510(k) number K890533. 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 ITEM #352/#CS352* CONTACT LENS CASES?

ITEM #352/#CS352* CONTACT LENS CASES is a medical device that received FDA 510(k) clearance on 1989-06-23. The listed applicant is Magnivision, Inc.. The 510(k) number is K890533.

When did ITEM #352/#CS352* CONTACT LENS CASES receive FDA 510(k) clearance?

ITEM #352/#CS352* CONTACT LENS CASES received FDA 510(k) clearance on 1989-06-23, under 510(k) number K890533.

Who is the listed applicant for ITEM #352/#CS352* CONTACT LENS CASES?

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

What is the FDA product code for ITEM #352/#CS352* CONTACT LENS CASES?

The FDA product code for ITEM #352/#CS352* CONTACT LENS CASES is LRX.

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Other records listing Magnivision, 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.

K900777ITEM #273 CONTACT LENS CASESK900778ITEM #272 MAGNIF-EYES CONTACT LENS CASEK897085COMFEES(R) + CON-PAK(TM) LENS CASEK897084CONFEES(R)+ CONTACT LENS HOLDERK882384DELUXE CONTACT LENS HOLDER (HARD & SOFT) #283K872567SOFT CONTACT LENS REMOVER

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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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