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GRICE FOOT PEDAL CONTROL/REDDICK IRRI/ASPIR SYST

K914913 Class I Traditional
Decision Date
1991-12-31
Sponsor / Applicant
Ideal Medical, Inc.

Technical Specification

510(k) Submission ID K914913
Product Code GDJ
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4800
Decision Date 1991-12-31
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

GRICE FOOT PEDAL CONTROL/REDDICK IRRI/ASPIR SYST received FDA 510(k) clearance under submission number K914913, sponsored by Ideal Medical, 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 1991-12-31.

Classification & Regulation

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