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FRAZIER-FERGUSON SUCTION TUBES (DISP.)

K801612 Class I Traditional
Decision Date
1980-08-04
Sponsor / Applicant
Edward Weck, Inc.

Technical Specification

510(k) Submission ID K801612
Product Code GCY
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4680
Decision Date 1980-08-04
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

FRAZIER-FERGUSON SUCTION TUBES (DISP.) received FDA 510(k) clearance under submission number K801612, sponsored by Edward Weck, 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 1980-08-04.

Classification & Regulation

This clearance is catalogued under FDA product code GCY and 21 CFR 878.4680, within the General, Plastic Surgery review panel as a Class I device.