meddevicedb.com FDA Device Reference

PROSPORE2 SELF-CONTAINED BIOLOGICAL INDICATOR

K994381 Class II Traditional
Decision Date
2001-03-30
Sponsor / Applicant
Raven Biological Laboratories, Inc.

Technical Specification

510(k) Submission ID K994381
Product Code FRC
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.2800
Decision Date 2001-03-30
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PROSPORE2 SELF-CONTAINED BIOLOGICAL INDICATOR received FDA 510(k) clearance under submission number K994381, sponsored by Raven Biological Laboratories, 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 2001-03-30.

Classification & Regulation

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