meddevicedb.com FDA Device Reference

I.V. PREP & CARE KIT

K771551 Class I Traditional
Decision Date
1977-10-04
Sponsor / Applicant
Jelco Laboratories

Technical Specification

510(k) Submission ID K771551
Product Code FRL
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5300
Decision Date 1977-10-04
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

I.V. PREP & CARE KIT received FDA 510(k) clearance under submission number K771551, sponsored by Jelco Laboratories. 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 1977-10-04.

Classification & Regulation

This clearance is catalogued under FDA product code FRL and 21 CFR 880.5300, within the General Hospital review panel as a Class I device.