meddevicedb.com FDA Device Reference

#1904L MUELLER HINTON W/5% SHEEP BLOOD

K820793 Class II Traditional
Decision Date
1982-04-08
Sponsor / Applicant
Biomedica, Inc.

Technical Specification

510(k) Submission ID K820793
Product Code JTZ
Medical Specialty / Panel Microbiology
Regulation Citation 21 CFR 866.1700
Decision Date 1982-04-08
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

#1904L MUELLER HINTON W/5% SHEEP BLOOD received FDA 510(k) clearance under submission number K820793, sponsored by Biomedica, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Microbiology review panel. The statutory decision date of record is 1982-04-08.

Classification & Regulation

This clearance is catalogued under FDA product code JTZ and 21 CFR 866.1700, within the Microbiology review panel as a Class II device.