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FDA 510(k)

DELUXE CONTACT LENS HOLDER (HARD & SOFT) #283

K-Number: K882384 · 1989-06-23

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

Device Summary

DELUXE CONTACT LENS HOLDER (HARD & SOFT) #283 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 K882384. 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 DELUXE CONTACT LENS HOLDER (HARD & SOFT) #283?

DELUXE CONTACT LENS HOLDER (HARD & SOFT) #283 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 K882384.

When did DELUXE CONTACT LENS HOLDER (HARD & SOFT) #283 receive FDA 510(k) clearance?

DELUXE CONTACT LENS HOLDER (HARD & SOFT) #283 received FDA 510(k) clearance on 1989-06-23, under 510(k) number K882384.

Who is the listed applicant for DELUXE CONTACT LENS HOLDER (HARD & SOFT) #283?

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 DELUXE CONTACT LENS HOLDER (HARD & SOFT) #283?

The FDA product code for DELUXE CONTACT LENS HOLDER (HARD & SOFT) #283 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 HOLDERK890533ITEM #352/#CS352* CONTACT LENS CASESK872567SOFT 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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