Product code LQO— Microbiology

FDA has cleared 4 devices under product code LQO between 1987 and 1989, filed by 4 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.

• 19891 clearance
• 19882 clearances
• 19871 clearance

• Wampole Laboratories1 clearance
• Molecular Biosystems, Inc.1 clearance
• Integrated Genetics1 clearance
• Gen-Probe, Inc.1 clearance

• K894712 — ACCUPROBE CAMPYLOBACTER CULTURE CONFIRMATIONGen-Probe, Inc.·1989-11-14
• K873670 — SNAP CAMPYLOBACTOR DIAGNOSTIC KITMolecular Biosystems, Inc.·1988-06-08
• K875101 — VIROGEN CMV ANTIBODY TESTWampole Laboratories·1988-03-01
• K863270 — GENE-TRAK CAMPYLOBACTER ASSAYIntegrated Genetics·1987-08-31