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FDA 510(k) Applications Submitted by ALERE SCARBOROUGH, INC
FDA 510(k) Number
Submission Date
Device Name
Applicant
K121905
06/29/2012
ALERE PBP2A TEST
ALERE SCARBOROUGH, INC
K141757
06/30/2014
ALERE I STREP A
ALERE SCARBOROUGH, INC
K123986
12/26/2012
ACTIM PROM
ALERE SCARBOROUGH, INC
K133851
12/19/2013
ALERE PBP2A SA/CONS CULTURE COLONY TEST
ALERE SCARBOROUGH, INC
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