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C-FLO SUCTION TUBE

K882121 Class II Traditional
Decision Date
1988-06-20
Sponsor / Applicant
Concept, Inc.

Technical Specification

510(k) Submission ID K882121
Product Code DXQ
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1120
Decision Date 1988-06-20
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

C-FLO SUCTION TUBE received FDA 510(k) clearance under submission number K882121, sponsored by Concept, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1988-06-20.

Classification & Regulation

This clearance is catalogued under FDA product code DXQ and 21 CFR 870.1120, within the Cardiovascular review panel as a Class II device.