meddevicedb.com FDA Device Reference

IV/0165 INFUSION SET

K851336 Class II Traditional
Decision Date
1985-05-30
Sponsor / Applicant
Infarkem Corp.

Technical Specification

510(k) Submission ID K851336
Product Code FPA
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5440
Decision Date 1985-05-30
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

IV/0165 INFUSION SET received FDA 510(k) clearance under submission number K851336, sponsored by Infarkem Corp.. 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 1985-05-30.

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.