510(k) K943812

VIDAS LYME SCREEN II by Biomerieux Vitek, Inc. — Product Code LSR

K943812 is an FDA 510(k) premarket notification submitted by Biomerieux Vitek, Inc. for the device "VIDAS LYME SCREEN II". The FDA issued a decision of Substantially Equivalent on June 13, 1995. The device falls under product code LSR (Reagent, Borrelia Serological Reagent), a Class II device regulated under 21 CFR 866.3830. Biomerieux Vitek, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
June 13, 1995
Date Received
August 5, 1994
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Reagent, Borrelia Serological Reagent
Device Class
Class II
Regulation Number
866.3830
Review Panel
MI
Submission Type