meddevicedb.com FDA Device Reference

REMEL CEFPROZIL 30 MCG SUSCEPTIBILITY DISK

K934100 Class II Traditional
Decision Date
1993-11-22
Sponsor / Applicant
Remel Co.

Technical Specification

510(k) Submission ID K934100
Product Code JTN
Medical Specialty / Panel Microbiology
Regulation Citation 21 CFR 866.1620
Decision Date 1993-11-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

REMEL CEFPROZIL 30 MCG SUSCEPTIBILITY DISK received FDA 510(k) clearance under submission number K934100, sponsored by Remel Co.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Microbiology review panel. The statutory decision date of record is 1993-11-22.

Classification & Regulation

This clearance is catalogued under FDA product code JTN and 21 CFR 866.1620, within the Microbiology review panel as a Class II device.