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SHUNT CONNECTORS

K893679 Class I Traditional
Decision Date
1989-07-24
Sponsor / Applicant
Akcess Medical Products, Inc.

Technical Specification

510(k) Submission ID K893679
Product Code FJQ
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5540
Decision Date 1989-07-24
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SHUNT CONNECTORS received FDA 510(k) clearance under submission number K893679, sponsored by Akcess Medical Products, 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 1989-07-24.

Classification & Regulation

This clearance is catalogued under FDA product code FJQ and 21 CFR 876.5540, within the Gastroenterology, Urology review panel as a Class I device.