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HUMPHREY FIELD ANALYZER MODEL 630

K852639 Class I Traditional
Decision Date
1985-09-18
Sponsor / Applicant
Zeiss Humphrey System

Technical Specification

510(k) Submission ID K852639
Product Code HPT
Medical Specialty / Panel Ophthalmic
Regulation Citation 21 CFR 886.1605
Decision Date 1985-09-18
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HUMPHREY FIELD ANALYZER MODEL 630 received FDA 510(k) clearance under submission number K852639, sponsored by Zeiss Humphrey System. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ophthalmic review panel. The statutory decision date of record is 1985-09-18.

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.