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ANGEL TIP SAFETY INTRAVASCULAR NEEDLE SET

K131950 Class II Traditional
Decision Date
2015-01-16
Sponsor / Applicant
Summit International Medical Technologies, Inc.

Technical Specification

510(k) Submission ID K131950
Product Code FIE
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5540
Decision Date 2015-01-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ANGEL TIP SAFETY INTRAVASCULAR NEEDLE SET received FDA 510(k) clearance under submission number K131950, sponsored by Summit International Medical Technologies, 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 2015-01-16.

Classification & Regulation

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