meddevicedb.com FDA Device Reference

DELTEC SUBCUTANEOUS INFUSION SET

K963009 Class II Traditional
Decision Date
1996-10-18
Sponsor / Applicant
Sims Deltec, Inc.

Technical Specification

510(k) Submission ID K963009
Product Code FPA
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5440
Decision Date 1996-10-18
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DELTEC SUBCUTANEOUS INFUSION SET received FDA 510(k) clearance under submission number K963009, sponsored by Sims Deltec, Inc.. 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 1996-10-18.

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.