meddevicedb.com FDA Device Reference

PROCHEM INDICATOR TAPE

K080307 Class II Traditional
Decision Date
2008-05-01
Sponsor / Applicant
Raven Laboratories

Technical Specification

510(k) Submission ID K080307
Product Code JOJ
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.2800
Decision Date 2008-05-01
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PROCHEM INDICATOR TAPE received FDA 510(k) clearance under submission number K080307, sponsored by Raven 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 2008-05-01.

Classification & Regulation

This clearance is catalogued under FDA product code JOJ and 21 CFR 880.2800, within the General Hospital review panel as a Class II device.