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MICROCAPILLARY INFUSION SYSTEM

K831347 Class II Traditional
Decision Date
1983-06-02
Sponsor / Applicant
J.S. Biomedicals, Inc.

Technical Specification

510(k) Submission ID K831347
Product Code FFX
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.1725
Decision Date 1983-06-02
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MICROCAPILLARY INFUSION SYSTEM received FDA 510(k) clearance under submission number K831347, sponsored by J.S. Biomedicals, 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 1983-06-02.

Classification & Regulation

This clearance is catalogued under FDA product code FFX and 21 CFR 876.1725, within the Gastroenterology, Urology review panel as a Class II device.