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PASCAL STREAMLINE PHOTOCOAGULATOR

K100019 Class II Traditional
Decision Date
2010-05-04
Sponsor / Applicant
Optimedica Corporation

Technical Specification

510(k) Submission ID K100019
Product Code HQF
Medical Specialty / Panel Ophthalmic
Regulation Citation 21 CFR 886.4390
Decision Date 2010-05-04
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PASCAL STREAMLINE PHOTOCOAGULATOR received FDA 510(k) clearance under submission number K100019, sponsored by Optimedica Corporation. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ophthalmic review panel. The statutory decision date of record is 2010-05-04.

Classification & Regulation

This clearance is catalogued under FDA product code HQF and 21 CFR 886.4390, within the Ophthalmic review panel as a Class II device.