Product code LQP— Microbiology

FDA has cleared 12 devices under product code LQP between 1986 and 2021, filed by 7 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.

• 20212 clearances
• 20192 clearances
• 20182 clearances
• 20092 clearances
• 19981 clearance
• 19881 clearance
• 19862 clearances

• Techlab, Inc.4 clearances
• Meridian Bioscience, Inc.3 clearances
• Quidel Corporation1 clearance
• Meridian Diagnostics, Inc.1 clearance
• Institute Virion , Ltd.1 clearance
• Bd Becton Dickinson Vacutainer Systems Preanalytic1 clearance
• Alexon - Trend, Inc.1 clearance

• K210976 — Curian CampyMeridian Bioscience, Inc.·2021-12-23
• K211342 — Sofia 2 Campylobacter FIAQuidel Corporation·2021-11-23
• K191442 — Campylobacter ChekTechlab, Inc.·2019-06-20
• K191456 — Campylobacter Quik ChekTechlab, Inc.·2019-06-20
• K173217 — CAMPYLOBACTER QUIK CHEKTechlab, Inc.·2018-01-22
• K173219 — CAMPYLOBACTER CHEKTechlab, Inc.·2018-01-22
• K090700 — IMMUNOCARD STAT CAMPY, MODEL 751530Meridian Bioscience, Inc.·2009-05-28
• K083464 — PREMIER CAMPY, MODEL 618096Meridian Bioscience, Inc.·2009-01-30
• K982315 — PROSPECT CAMPYLOBACTER MICROPLATE ASSAYAlexon - Trend, Inc.·1998-11-18
• K880389 — MERITEC(TM)-CAMPY (JCL)Meridian Diagnostics, Inc.·1988-04-12
• K864027 — BBL CAMPYSLIDE(TM) TESTBd Becton Dickinson Vacutainer Systems Preanalytic·1986-12-11
• K862814 — COMPLEMENT-FIXATION TEST FOR CAMPYLOBACTER JEJUNIInstitute Virion , Ltd.·1986-09-30