510(k) K892206

MARDX LLYME DISEASE EIA (IGG & IGM) TEST SYSTEM by Mardx Diagnostics, Inc. — Product Code LSR

K892206 is an FDA 510(k) premarket notification submitted by Mardx Diagnostics, Inc. for the device "MARDX LLYME DISEASE EIA (IGG & IGM) TEST SYSTEM". The FDA issued a decision of Substantially Equivalent on August 15, 1989. The device falls under product code LSR (Reagent, Borrelia Serological Reagent), a Class II device regulated under 21 CFR 866.3830. Mardx Diagnostics, Inc. has at least 7 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 15, 1989
Date Received
April 3, 1989
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