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HARDYDISK AST CEFTAROLINE, 30 UG MODEL Z939

K103538 Class II Traditional
Decision Date
2010-12-17
Sponsor / Applicant
Hardy Diagnostics

Technical Specification

510(k) Submission ID K103538
Product Code JTN
Medical Specialty / Panel Microbiology
Regulation Citation 21 CFR 866.1620
Decision Date 2010-12-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HARDYDISK AST CEFTAROLINE, 30 UG MODEL Z939 received FDA 510(k) clearance under submission number K103538, 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 2010-12-17.

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.