FDA 510(k) Applications Submitted by PAM ANGELL

FDA 510(k) Number Submission Date Device Name Applicant
K041049 04/22/2004 BINAXNOW INFLUENZA A & B TEST BINAX, INC.
K032166 07/16/2003 BINAX NOW RSV TEST, MODEL 430-000 AND BINAX NOW NASOPHARYNGEAL SWAB ACCESSORY PACK, MODEL 400-065 BINAX, INC.
K012521 08/06/2001 BINAX NOW STREPTOCOCCUS PNEUMONIAE TEST BINAX, INC.
K960712 02/21/1996 BINAX STREP A TEST BINAX, INC.
K010523 02/22/2001 MODIFICATION TO BINAX NOW STREPTOCOCCUS PNEUMONIAE URINARY ANTIGEN TEST BINAX, INC.
K991726 05/20/1999 BINAX NOWR STREPTOCOCCUS PNEUMONIAE URINARY ANTIGEN TEST (22 TEST KIT),(12 TEST KIT), BINAX NOWR STREPTOCOCCUS PNEUMONI BINAX, INC.
K982238 06/25/1998 BINAX NOW LEGIONELLA URINARY ANTIGEN TEST MODEL 852-020 AND BINAX NOW LEG IONELLA URINARY ANTIGEN CONTROL KIT MODEL 8522 BINAX, INC.


Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact