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SOLA SCHULTZE-CROCK OPTHALMOSCOPE

K760771 Class II Traditional
Decision Date
1976-10-15
Sponsor / Applicant
Codman & Shurtleff, Inc.

Technical Specification

510(k) Submission ID K760771
Product Code HLJ
Medical Specialty / Panel Ophthalmic
Regulation Citation 21 CFR 886.1570
Decision Date 1976-10-15
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SOLA SCHULTZE-CROCK OPTHALMOSCOPE received FDA 510(k) clearance under submission number K760771, sponsored by Codman & Shurtleff, 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 1976-10-15.

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.