meddevicedb.com FDA Device Reference

TRANSPORT CULTURE MEDIUM

K850737 Class I Traditional
Decision Date
1985-03-20
Sponsor / Applicant
Roseville Medical Laboratoriesu

Technical Specification

510(k) Submission ID K850737
Product Code PPM
Medical Specialty / Panel Pathology
Regulation Citation 21 CFR 864.4010
Decision Date 1985-03-20
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TRANSPORT CULTURE MEDIUM received FDA 510(k) clearance under submission number K850737, sponsored by Roseville Medical Laboratoriesu. The device was reviewed via the Traditional premarket notification pathway and assigned to the Pathology review panel. The statutory decision date of record is 1985-03-20.

Classification & Regulation

This clearance is catalogued under FDA product code PPM and 21 CFR 864.4010, within the Pathology review panel as a Class I device.