meddevicedb.com FDA Device Reference

PERMA-SET INFUSION SET

K822603 Class II Traditional
Decision Date
1982-09-14
Sponsor / Applicant
Cosmetic Sciences, Inc.

Technical Specification

510(k) Submission ID K822603
Product Code LDR
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5725
Decision Date 1982-09-14
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PERMA-SET INFUSION SET received FDA 510(k) clearance under submission number K822603, sponsored by Cosmetic Sciences, 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 1982-09-14.

Classification & Regulation

This clearance is catalogued under FDA product code LDR and 21 CFR 880.5725, within the General Hospital review panel as a Class II device.