meddevicedb.com FDA Device Reference

CHEMO-SHIELD

K897105 Class II Traditional
Decision Date
1990-03-19
Sponsor / Applicant
Vision Plastics, Inc.

Technical Specification

510(k) Submission ID K897105
Product Code FMF
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5860
Decision Date 1990-03-19
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CHEMO-SHIELD received FDA 510(k) clearance under submission number K897105, sponsored by Vision Plastics, 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 1990-03-19.

Classification & Regulation

This clearance is catalogued under FDA product code FMF and 21 CFR 880.5860, within the General Hospital review panel as a Class II device.