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FDA 510(k)

HARD CONTACT LENS REMOVER. ITEM #289

K-Number: K872591 · 1987-08-04

ApplicantMagnivision, Inc.
Decision Date1987-08-04
Product CodeKYE
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

HARD CONTACT LENS REMOVER. ITEM #289 is the device name listed in this FDA 510(k) record. The listed applicant is Magnivision, Inc.. It received FDA 510(k) clearance on 1987-08-04 under 510(k) number K872591. The device is classified under product code KYE. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HARD CONTACT LENS REMOVER. ITEM #289?

HARD CONTACT LENS REMOVER. ITEM #289 is a medical device that received FDA 510(k) clearance on 1987-08-04. The listed applicant is Magnivision, Inc.. The 510(k) number is K872591.

When did HARD CONTACT LENS REMOVER. ITEM #289 receive FDA 510(k) clearance?

HARD CONTACT LENS REMOVER. ITEM #289 received FDA 510(k) clearance on 1987-08-04, under 510(k) number K872591.

Who is the listed applicant for HARD CONTACT LENS REMOVER. ITEM #289?

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 HARD CONTACT LENS REMOVER. ITEM #289?

The FDA product code for HARD CONTACT LENS REMOVER. ITEM #289 is KYE.

Related Clinical Trials

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

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 CASESK882384DELUXE CONTACT LENS HOLDER (HARD & SOFT) #283

View all 8 devices →

Related Devices (Code: KYE)

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.

K872567SOFT CONTACT LENS REMOVERMagnivision, Inc.K871130CONTACT LENS TWEEZERSS. M. C. Medi-Tech Corp.K870072SUMMIT OPTICS CONTACT LENS REMOVERDayton Mfg. Co.K850984MARLIN SOFT LENS HANDLERMarlin IndustriesK850983MARLIN SOFT LENS TWEEZERMarlin IndustriesK830738LENSERT CONTACT LENS CLEANING & INSERTJermyn Specialties of California

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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