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ELECTRIC INSTRUMENT TABLE

K832073 Class I Traditional
Decision Date
1983-08-12
Sponsor / Applicant
CooperVision, Inc.

Technical Specification

510(k) Submission ID K832073
Product Code HMF
Medical Specialty / Panel Ophthalmic
Regulation Citation 21 CFR 886.1860
Decision Date 1983-08-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ELECTRIC INSTRUMENT TABLE received FDA 510(k) clearance under submission number K832073, sponsored by CooperVision, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ophthalmic review panel. The statutory decision date of record is 1983-08-12.

Classification & Regulation

This clearance is catalogued under FDA product code HMF and 21 CFR 886.1860, within the Ophthalmic review panel as a Class I device.