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KEATES I/A SYSTEM FRIGITRONICS 4000

K822599 Class II Traditional
Decision Date
1982-10-06
Sponsor / Applicant
Frigitronics of Connecticut, Inc.

Technical Specification

510(k) Submission ID K822599
Product Code HKP
Medical Specialty / Panel Ophthalmic
Regulation Citation 21 CFR 886.4150
Decision Date 1982-10-06
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

KEATES I/A SYSTEM FRIGITRONICS 4000 received FDA 510(k) clearance under submission number K822599, sponsored by Frigitronics of Connecticut, 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 1982-10-06.

Classification & Regulation

This clearance is catalogued under FDA product code HKP and 21 CFR 886.4150, within the Ophthalmic review panel as a Class II device.