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FDA 510(k)

MARLIN SOFT LENS TWEEZER

K-Number: K850983 · 1985-09-10

ApplicantMarlin Industries
Decision Date1985-09-10
Product CodeKYE
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

MARLIN SOFT LENS TWEEZER is the device name listed in this FDA 510(k) record. The listed applicant is Marlin Industries. It received FDA 510(k) clearance on 1985-09-10 under 510(k) number K850983. 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 MARLIN SOFT LENS TWEEZER?

MARLIN SOFT LENS TWEEZER is a medical device that received FDA 510(k) clearance on 1985-09-10. The listed applicant is Marlin Industries. The 510(k) number is K850983.

When did MARLIN SOFT LENS TWEEZER receive FDA 510(k) clearance?

MARLIN SOFT LENS TWEEZER received FDA 510(k) clearance on 1985-09-10, under 510(k) number K850983.

Who is the listed applicant for MARLIN SOFT LENS TWEEZER?

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

What is the FDA product code for MARLIN SOFT LENS TWEEZER?

The FDA product code for MARLIN SOFT LENS TWEEZER 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 Marlin Industries 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.

K850984MARLIN SOFT LENS HANDLERK851497MARLIN 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.K870072SUMMIT OPTICS CONTACT LENS REMOVERDayton Mfg. Co.K850984MARLIN SOFT LENS HANDLERMarlin 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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