Product code LJF— Microbiology

FDA has cleared 4 devices under product code LJF between 1982 and 2000, filed by 3 applicant companies. No FDA device recalls reference this product code. Class I devices are low-risk and subject to FDA general controls; many Class I device types are exempt from 510(k) premarket notification.

• 20001 clearance
• 19832 clearances
• 19821 clearance

• Marion Laboratories, Inc.2 clearances
• Organon Teknika Corp.1 clearance
• Bd Becton Dickinson Vacutainer Systems Preanalytic1 clearance

• K003104 — BACT/ALERT CSROrganon Teknika Corp.·2000-10-20
• K830372 — ARTIMICROBIAL REMOVAL DEVICEMarion Laboratories, Inc.·1983-04-08
• K830363 — BACTEC 170 TRYPTIC SOY BROTH W/RESINSBd Becton Dickinson Vacutainer Systems Preanalytic·1983-03-24
• K822344 — ANTIMICROBIAL REMOVAL DEVICE (ARD)Marion Laboratories, Inc.·1982-08-25