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HALOGEN OPHTHALMO-OTOSCOPE SET BX A - 134

K950797 Class II Traditional
Decision Date
1995-03-28
Sponsor / Applicant
Neitz Instruments Company, Ltd.

Technical Specification

510(k) Submission ID K950797
Product Code HLJ
Medical Specialty / Panel Ophthalmic
Regulation Citation 21 CFR 886.1570
Decision Date 1995-03-28
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HALOGEN OPHTHALMO-OTOSCOPE SET BX A - 134 received FDA 510(k) clearance under submission number K950797, sponsored by Neitz Instruments Company, Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ophthalmic review panel. The statutory decision date of record is 1995-03-28.

Classification & Regulation

This clearance is catalogued under FDA product code HLJ and 21 CFR 886.1570, within the Ophthalmic review panel as a Class II device.