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MICROSURGE SUCTION/IRRIGATION SYSTEM CANNULAS

K930355 Class II Traditional
Decision Date
1993-06-08
Sponsor / Applicant
Microsurge, Inc.

Technical Specification

510(k) Submission ID K930355
Product Code GEI
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4400
Decision Date 1993-06-08
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MICROSURGE SUCTION/IRRIGATION SYSTEM CANNULAS received FDA 510(k) clearance under submission number K930355, sponsored by Microsurge, 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 1993-06-08.

Classification & Regulation

This clearance is catalogued under FDA product code GEI and 21 CFR 878.4400, within the General, Plastic Surgery review panel as a Class II device.