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MEDCOMP FEMORAL VEIN CATHETER

K801967 Class II Traditional
Decision Date
1980-09-26
Sponsor / Applicant
Medical Components, Inc.

Technical Specification

510(k) Submission ID K801967
Product Code FIF
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5820
Decision Date 1980-09-26
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MEDCOMP FEMORAL VEIN CATHETER received FDA 510(k) clearance under submission number K801967, sponsored by Medical Components, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Gastroenterology, Urology review panel. The statutory decision date of record is 1980-09-26.

Classification & Regulation

This clearance is catalogued under FDA product code FIF and 21 CFR 876.5820, within the Gastroenterology, Urology review panel as a Class II device.