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SIMPLA TRIDENT LEG BAG + SIMPLA S6 BAG

K925067 Class II Traditional
Decision Date
1993-06-10
Sponsor / Applicant
Simport Plastics, Ltd.

Technical Specification

510(k) Submission ID K925067
Product Code KNX
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5250
Decision Date 1993-06-10
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SIMPLA TRIDENT LEG BAG + SIMPLA S6 BAG received FDA 510(k) clearance under submission number K925067, sponsored by Simport Plastics, Ltd.. 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 1993-06-10.

Classification & Regulation

This clearance is catalogued under FDA product code KNX and 21 CFR 876.5250, within the Gastroenterology, Urology review panel as a Class II device.