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MARLIN SOFT LENS HANDLER

K850984 Class I Traditional
Decision Date
1985-09-10
Sponsor / Applicant
Marlin Industries

Technical Specification

510(k) Submission ID K850984
Product Code KYE
Medical Specialty / Panel Ophthalmic
Regulation Citation 21 CFR 886.5420
Decision Date 1985-09-10
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MARLIN SOFT LENS HANDLER received FDA 510(k) clearance under submission number K850984, sponsored by Marlin Industries. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ophthalmic review panel. The statutory decision date of record is 1985-09-10.

Classification & Regulation

This clearance is catalogued under FDA product code KYE and 21 CFR 886.5420, within the Ophthalmic review panel as a Class I device.