meddevicedb.com FDA Device Reference

INTRAVASCULAR ADMINISTRATION SET

K140175 Class II Traditional
Decision Date
2014-08-05
Sponsor / Applicant
Delta Med Spa

Technical Specification

510(k) Submission ID K140175
Product Code FPA
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5440
Decision Date 2014-08-05
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

INTRAVASCULAR ADMINISTRATION SET received FDA 510(k) clearance under submission number K140175, sponsored by Delta Med Spa. 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 2014-08-05.

Classification & Regulation

This clearance is catalogued under FDA product code FPA and 21 CFR 880.5440, within the General Hospital review panel as a Class II device.