510(k) K123256

HUMAN ALPHA-1 ANTITRYPSIN KIT SPAPLUS by The Binding Site Group , Ltd. — Product Code DEM

K123256 is an FDA 510(k) premarket notification submitted by The Binding Site Group , Ltd. for the device "HUMAN ALPHA-1 ANTITRYPSIN KIT SPAPLUS". The FDA issued a decision of Substantially Equivalent on July 3, 2013. The device falls under product code DEM (Alpha-1-Antitrypsin, Antigen, Antiserum, Control), a Class II device regulated under 21 CFR 866.5130. The Binding Site Group , Ltd. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
July 3, 2013
Date Received
October 18, 2012
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Alpha-1-Antitrypsin, Antigen, Antiserum, Control
Device Class
Class II
Regulation Number
866.5130
Review Panel
IM
Submission Type