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FDA 510(k)

SUMMIT OPTICS CONTACT LENS REMOVER

K-Number: K870072 · 1987-02-12

ApplicantDayton Mfg. Co.
Decision Date1987-02-12
Product CodeKYE
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

SUMMIT OPTICS CONTACT LENS REMOVER is the device name listed in this FDA 510(k) record. The listed applicant is Dayton Mfg. Co.. It received FDA 510(k) clearance on 1987-02-12 under 510(k) number K870072. 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 SUMMIT OPTICS CONTACT LENS REMOVER?

SUMMIT OPTICS CONTACT LENS REMOVER is a medical device that received FDA 510(k) clearance on 1987-02-12. The listed applicant is Dayton Mfg. Co.. The 510(k) number is K870072.

When did SUMMIT OPTICS CONTACT LENS REMOVER receive FDA 510(k) clearance?

SUMMIT OPTICS CONTACT LENS REMOVER received FDA 510(k) clearance on 1987-02-12, under 510(k) number K870072.

Who is the listed applicant for SUMMIT OPTICS CONTACT LENS REMOVER?

The FDA 510(k) record lists Dayton Mfg. Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SUMMIT OPTICS CONTACT LENS REMOVER?

The FDA product code for SUMMIT OPTICS CONTACT LENS REMOVER 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 Dayton Mfg. Co. 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.

K870164SUMMIT OPTICS SOFT CONTACT LENS CASE

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.K872591HARD CONTACT LENS REMOVER. ITEM #289Magnivision, Inc.K871130CONTACT LENS TWEEZERSS. M. C. Medi-Tech Corp.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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