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IMAGENET DIGITAL OPHTHALMIC IMAGING SYSTEM

K870039 Class I Traditional
Decision Date
1987-02-12
Sponsor / Applicant
Par Microsystems Corp.

Technical Specification

510(k) Submission ID K870039
Product Code DSF
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.2810
Decision Date 1987-02-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

IMAGENET DIGITAL OPHTHALMIC IMAGING SYSTEM received FDA 510(k) clearance under submission number K870039, sponsored by Par Microsystems Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1987-02-12.

Classification & Regulation

This clearance is catalogued under FDA product code DSF and 21 CFR 870.2810, within the Cardiovascular review panel as a Class I device.