510(k) K974809

ACCURUN(TM) 130 BORRELIA BURGDORFERI IGG POSITIVE CONTROL by Boston Biomedica, Inc. — Product Code LSR

K974809 is an FDA 510(k) premarket notification submitted by Boston Biomedica, Inc. for the device "ACCURUN(TM) 130 BORRELIA BURGDORFERI IGG POSITIVE CONTROL". The FDA issued a decision of Substantially Equivalent on February 5, 1998. The device falls under product code LSR (Reagent, Borrelia Serological Reagent), a Class II device regulated under 21 CFR 866.3830. Boston Biomedica, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 5, 1998
Date Received
December 23, 1997
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