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ANOMALOSCOPE PLATE TEST - 5 [APT-5]

K875026 Class I Traditional
Decision Date
1988-02-05
Sponsor / Applicant
Lkc Technologies, Inc.

Technical Specification

510(k) Submission ID K875026
Product Code HIT
Medical Specialty / Panel Ophthalmic
Regulation Citation 21 CFR 886.1170
Decision Date 1988-02-05
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ANOMALOSCOPE PLATE TEST - 5 [APT-5] received FDA 510(k) clearance under submission number K875026, sponsored by Lkc Technologies, 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 1988-02-05.

Classification & Regulation

This clearance is catalogued under FDA product code HIT and 21 CFR 886.1170, within the Ophthalmic review panel as a Class I device.