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DIGILAB 750 AUTOMATED PERIMETER W/IBM PERSON/COMPU

K850191 Class I Traditional
Decision Date
1985-03-04
Sponsor / Applicant
Bio-Rad

Technical Specification

510(k) Submission ID K850191
Product Code HPT
Medical Specialty / Panel Ophthalmic
Regulation Citation 21 CFR 886.1605
Decision Date 1985-03-04
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DIGILAB 750 AUTOMATED PERIMETER W/IBM PERSON/COMPU received FDA 510(k) clearance under submission number K850191, sponsored by Bio-Rad. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ophthalmic review panel. The statutory decision date of record is 1985-03-04.

Classification & Regulation

This clearance is catalogued under FDA product code HPT and 21 CFR 886.1605, within the Ophthalmic review panel as a Class I device.