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IRRIGATION CATHETER

K780788 Class I Traditional
Decision Date
1978-06-22
Sponsor / Applicant
Shiley, Inc.

Technical Specification

510(k) Submission ID K780788
Product Code GBX
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4200
Decision Date 1978-06-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

IRRIGATION CATHETER received FDA 510(k) clearance under submission number K780788, sponsored by Shiley, 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 1978-06-22.

Classification & Regulation

This clearance is catalogued under FDA product code GBX and 21 CFR 878.4200, within the General, Plastic Surgery review panel as a Class I device.