Product code LQL— Microbiology

FDA has cleared 11 devices under product code LQL between 1986 and 1998, filed by 10 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.

• 19981 clearance
• 19972 clearances
• 19961 clearance
• 19931 clearance
• 19912 clearances
• 19901 clearance
• 19891 clearance
• 19881 clearance
• 19861 clearance

• Biomerieux Vitek, Inc.2 clearances
• Vitek Systems, Inc.1 clearance
• Mct Medical, Inc.1 clearance
• Kev Connecticut Diagnostics, Inc.1 clearance
• Dms Products, Inc.1 clearance
• Becton Dickinson Microbiology Systems1 clearance
• Bd Becton Dickinson Vacutainer Systems Preanalytic1 clearance
• Analytical Products, Inc.1 clearance
• American Micro Scan1 clearance
• Accumed Intl., Inc.1 clearance

• K972576 — GRAM POSITIVE AUTOIDENTIFICATION PLATES, SENSITITRE AP90Accumed Intl., Inc.·1998-01-22
• K961730 — RAPID GRAM-POSITIVE ID SYSTEMBecton Dickinson Microbiology Systems·1997-02-04
• K961968 — BBLCRYSTAL GRAM-POSITIVE ID SYSTEMBd Becton Dickinson Vacutainer Systems Preanalytic·1997-02-04
• K952095 — VITEK GRAM POSITIVE IDENTIFICATION CARD (GPI)Biomerieux Vitek, Inc.·1996-03-12
• K925916 — VITEK RAPID CALL-GRAM POSITIVE IDENTIFICATION CARDBiomerieux Vitek, Inc.·1993-03-23
• K910304 — RAPID CORYNE SYST/IDENTIF OF CORYNEFORM BACTERIAVitek Systems, Inc.·1991-07-26
• K910537 — VISI-STREPKev Connecticut Diagnostics, Inc.·1991-04-12
• K901559 — MODIFICATION TO API UNISCEPT 20GPAnalytical Products, Inc.·1990-09-10
• K891004 — RAPIDEC STAPHDms Products, Inc.·1989-11-09
• K874606 — CATHRA GRAM POSITIVE SCREENMct Medical, Inc.·1988-05-06
• K863038 — GRAM POSITIVE FLUORESCENT IDENTIFICATION PANELAmerican Micro Scan·1986-09-30