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FDA 510(k)

DMV ANGLER

K-Number: K830496 · 1983-03-09

ApplicantDmv Contact Lens Co.
Decision Date1983-03-09
Product CodeKYE
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

DMV ANGLER is the device name listed in this FDA 510(k) record. The listed applicant is Dmv Contact Lens Co.. It received FDA 510(k) clearance on 1983-03-09 under 510(k) number K830496. 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 DMV ANGLER?

DMV ANGLER is a medical device that received FDA 510(k) clearance on 1983-03-09. The listed applicant is Dmv Contact Lens Co.. The 510(k) number is K830496.

When did DMV ANGLER receive FDA 510(k) clearance?

DMV ANGLER received FDA 510(k) clearance on 1983-03-09, under 510(k) number K830496.

Who is the listed applicant for DMV ANGLER?

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

What is the FDA product code for DMV ANGLER?

The FDA product code for DMV ANGLER 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 Dmv Contact Lens 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.

K780664SOFT LENS REMOVER/INSERTER/MANIPULATORK780663CONTACT LENS REMOVER AND INSERTER

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.K870072SUMMIT OPTICS CONTACT LENS REMOVERDayton Mfg. Co.K850984MARLIN SOFT LENS HANDLERMarlin IndustriesK850983MARLIN SOFT LENS TWEEZERMarlin Industries

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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