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CATHETER METAL HUB/NONRADIOPAQUE

K790968 Class II Traditional
Decision Date
1979-06-11
Sponsor / Applicant
Jelco Laboratories

Technical Specification

510(k) Submission ID K790968
Product Code FOZ
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5200
Decision Date 1979-06-11
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CATHETER METAL HUB/NONRADIOPAQUE received FDA 510(k) clearance under submission number K790968, sponsored by Jelco Laboratories. The device was reviewed via the Traditional premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 1979-06-11.

Classification & Regulation

This clearance is catalogued under FDA product code FOZ and 21 CFR 880.5200, within the General Hospital review panel as a Class II device.