FDA 510(k) Applications for Medical Device Product Code "GLQ"
(Mixture, Control, White-Cell And Red-Cell Indices)

FDA 510(k) Number Applicant Device Name Decision Date
K101335 Streck CELL-CHEX 08/23/2010
K110718 Streck CELL-CHEX WITH CPPD CRYSTALS 05/26/2011
K111211 Streck CELL-DYN 22 PLUS CONTROL 12/22/2011
K090137 Streck STAK-CHEX PLUS RETICS 03/18/2009
K000945 STRECK LABORATORIES, INC. PARA 12 PLUS RETICS 04/18/2000
K992887 STRECK LABORATORIES, INC. STAK-CHEX PLUS RETICS 11/22/1999
K994388 STRECK LABORATORIES, INC. XE CHECK 01/14/2000


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