meddevicedb.com FDA Device Reference

HARDYDISK RIFAMPIN, 5MCG

K003537 Class II Traditional
Decision Date
2001-01-12
Sponsor / Applicant
Hardy Diagnostics

Technical Specification

510(k) Submission ID K003537
Product Code JTN
Medical Specialty / Panel Microbiology
Regulation Citation 21 CFR 866.1620
Decision Date 2001-01-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HARDYDISK RIFAMPIN, 5MCG received FDA 510(k) clearance under submission number K003537, sponsored by Hardy Diagnostics. The device was reviewed via the Traditional premarket notification pathway and assigned to the Microbiology review panel. The statutory decision date of record is 2001-01-12.

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.