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ETEST CEFDITOREN FOR S. PNEUMONIAE AND H. INFLUENZAE

K021445 Class II Traditional
Decision Date
2002-06-06
Sponsor / Applicant
Ab Biodisk

Technical Specification

510(k) Submission ID K021445
Product Code JWY
Medical Specialty / Panel Microbiology
Regulation Citation 21 CFR 866.1640
Decision Date 2002-06-06
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ETEST CEFDITOREN FOR S. PNEUMONIAE AND H. INFLUENZAE received FDA 510(k) clearance under submission number K021445, sponsored by Ab Biodisk. The device was reviewed via the Traditional premarket notification pathway and assigned to the Microbiology review panel. The statutory decision date of record is 2002-06-06.

Classification & Regulation

This clearance is catalogued under FDA product code JWY and 21 CFR 866.1640, within the Microbiology review panel as a Class II device.