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IRRIGATOR/ASPIRATOR PROBE

K915074 Class I Traditional
Decision Date
1992-02-05
Sponsor / Applicant
Biomedical Dynamics, Inc.

Technical Specification

510(k) Submission ID K915074
Product Code HMX
Medical Specialty / Panel Ophthalmic
Regulation Citation 21 CFR 886.4350
Decision Date 1992-02-05
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

IRRIGATOR/ASPIRATOR PROBE received FDA 510(k) clearance under submission number K915074, sponsored by Biomedical Dynamics, 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 1992-02-05.

Classification & Regulation

This clearance is catalogued under FDA product code HMX and 21 CFR 886.4350, within the Ophthalmic review panel as a Class I device.