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PROCEDURE TRAY/FOR VARIOUS OPHTHALMIC PROCEDURES

K905462 Class I Traditional
Decision Date
1991-02-06
Sponsor / Applicant
Angiosystems, Inc.

Technical Specification

510(k) Submission ID K905462
Product Code LRP
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4800
Decision Date 1991-02-06
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PROCEDURE TRAY/FOR VARIOUS OPHTHALMIC PROCEDURES received FDA 510(k) clearance under submission number K905462, sponsored by Angiosystems, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 1991-02-06.

Classification & Regulation

This clearance is catalogued under FDA product code LRP and 21 CFR 878.4800, within the General, Plastic Surgery review panel as a Class I device.