Product code LRH— Microbiology

FDA has cleared 4 devices under product code LRH between 1992 and 1996, 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.

• 19962 clearances
• 19941 clearance
• 19921 clearance

• Dade Microscan, Inc.1 clearance
• Biomerieux Vitek, Inc.1 clearance
• Bd Becton Dickinson Vacutainer Systems Preanalytic1 clearance
• Alamar Biosciences Laboratory, Inc.1 clearance

• K962609 — GRAM NEGATIVE IDENTIFICATION PLUS CARDBiomerieux Vitek, Inc.·1996-08-30
• K961042 — MICROSCAN RAPID GRAM-NEGATIVE INDENTIFICATION TYPE 3 PANELDade Microscan, Inc.·1996-05-30
• K926248 — READERAlamar Biosciences Laboratory, Inc.·1994-05-17
• K920225 — AUTOSCEPTOR IDENTIFICATION SYSTEMBd Becton Dickinson Vacutainer Systems Preanalytic·1992-05-22