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VITRECTOMY INTEGRATING TRAY OCUTOME/FRAG

K791212 Class II Traditional
Decision Date
1979-08-10
Sponsor / Applicant
Precision Medical Instruments, Inc.

Technical Specification

510(k) Submission ID K791212
Product Code HQE
Medical Specialty / Panel Ophthalmic
Regulation Citation 21 CFR 886.4150
Decision Date 1979-08-10
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

VITRECTOMY INTEGRATING TRAY OCUTOME/FRAG received FDA 510(k) clearance under submission number K791212, sponsored by Precision Medical Instruments, 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 1979-08-10.

Classification & Regulation

This clearance is catalogued under FDA product code HQE and 21 CFR 886.4150, within the Ophthalmic review panel as a Class II device.