510(k) K082329

VIRAMED BIOTECH AG BORRELIA B31 IGM VIRASTRIPE by Viramed Biotech AG — Product Code LSR

K082329 is an FDA 510(k) premarket notification submitted by Viramed Biotech AG for the device "VIRAMED BIOTECH AG BORRELIA B31 IGM VIRASTRIPE". The FDA issued a decision of Substantially Equivalent on August 5, 2009. The device falls under product code LSR (Reagent, Borrelia Serological Reagent), a Class II device regulated under 21 CFR 866.3830. Viramed Biotech AG has at least 6 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 5, 2009
Date Received
August 14, 2008
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